Linked Data
ClinVar Variation Id:
128775
dbSNP Id:
rs146610181
ExAC:
16:28488944 G / T
gnomAD v2:
16-28488944-G-T
gnomAD v3:
16-28477623-G-T
gnomAD v4:
16-28477623-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.28477623G>T , CM000678.2:g.28477623G>T | GRCh38 |
| NC_000016.9:g.28488944G>T , CM000678.1:g.28488944G>T | GRCh37 |
| NC_000016.8:g.28396445G>T | NCBI36 |
| NG_008654.2:g.19680C>A , LRG_689:g.19680C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000333496.14:c.1138C>A | ENSP00000329171.9:p.His380Asn | |
| ENST00000355477.10:c.1066C>A | ENSP00000347660.7:p.His356Asn | |
| ENST00000357857.14:c.1048C>A | ENSP00000350523.9:p.His350Asn | |
| ENST00000359984.12:c.1210C>A | ENSP00000353073.9:p.His404Asn | |
| ENST00000360019.8:c.1138C>A | ENSP00000353116.3:p.His380Asn | |
| ENST00000395653.9:c.751C>A | ENSP00000379014.5:p.His251Asn | |
| ENST00000561689.6:n.1623C>A | ||
| ENST00000564091.6:c.550C>A | ENSP00000454466.2:p.His184Asn | |
| ENST00000565316.6:c.1159C>A | ENSP00000456117.1:p.His387Asn | |
| ENST00000567963.6:c.1048C>A | ENSP00000455387.2:p.His350Asn | |
| ENST00000568076.6:n.1639C>A | ||
| ENST00000568422.6:c.*447C>A | ENSP00000455549.2:n.*447C>A | |
| ENST00000568452.6:n.1441C>A | ||
| ENST00000569430.7:c.1210C>A | ENSP00000454229.1:p.His404Asn | |
| ENST00000628023.3:c.*506C>A | ENSP00000486178.1:n.*506C>A | |
| ENST00000635861.1:c.*862C>A | ENSP00000490034.1:n.*862C>A | |
| ENST00000635887.1:c.1210C>A | ENSP00000490709.1:p.His404Asn | |
| ENST00000635958.1:n.1617C>A | ||
| ENST00000636017.1:c.*734C>A | ENSP00000490538.1:n.*734C>A | |
| ENST00000636078.1:n.1332C>A | ||
| ENST00000636147.2:c.1210C>A MANE Select | ENSP00000490105.1:p.His404Asn | |
| ENST00000636172.1:c.*734C>A | ENSP00000490505.1:n.*734C>A | |
| ENST00000636228.1:c.904C>A | ENSP00000489627.1:p.His302Asn | |
| ENST00000636351.1:n.1104C>A | ||
| ENST00000636503.1:c.*240C>A | ENSP00000489824.1:n.*240C>A | |
| ENST00000636766.1:c.1210C>A | ENSP00000489841.1:p.His404Asn | |
| ENST00000636839.1:n.1706C>A | ||
| ENST00000636853.1:n.2223C>A | ||
| ENST00000636866.1:c.*5C>A | ENSP00000490880.1:n.*5C>A | |
| ENST00000636907.1:n.1361C>A | ||
| ENST00000636977.1:n.2702C>A | ||
| ENST00000637050.1:n.1599C>A | ||
| ENST00000637100.1:c.1006-3361C>A | ENSP00000490394.1:n.1006-3361C>A | |
| ENST00000637107.1:c.*734C>A | ENSP00000490248.1:n.*734C>A | |
| ENST00000637184.1:c.*240C>A | ENSP00000489952.1:n.*240C>A | |
| ENST00000637299.1:c.*1019C>A | ENSP00000489823.1:n.*1019C>A | |
| ENST00000637376.1:c.*240C>A | ENSP00000490758.1:n.*240C>A | |
| ENST00000637378.1:c.228+4482C>A | ENSP00000490831.1:n.228+4482C>A | |
| ENST00000637578.1:c.*734C>A | ENSP00000490206.1:n.*734C>A | |
| ENST00000637699.1:c.1121C>A | ENSP00000490049.1:n.1121C>A | |
| ENST00000637745.1:c.647C>A | ||
| ENST00000637871.1:c.*908C>A | ENSP00000490670.1:n.*908C>A | |
| ENST00000638036.1:c.372C>A | ||
| ENST00000333496.13:c.1138C>A | ENSP00000329171.9:p.His380Asn | |
| ENST00000355477.9:c.*447C>A | ENSP00000347660.6:n.*447C>A | |
| ENST00000357806.11:c.913C>A | ENSP00000350457.7:p.His305Asn | |
| ENST00000357857.13:c.1048C>A | ENSP00000350523.9:p.His350Asn | |
| ENST00000359984.11:c.904C>A | ENSP00000353073.8:p.His302Asn | |
| ENST00000360019.6:c.1210C>A | ENSP00000353116.2:p.His404Asn | |
| ENST00000395653.8:c.910C>A | ENSP00000379014.4:p.His304Asn | |
| ENST00000561689.5:n.1179C>A | ||
| ENST00000563874.5:n.2738C>A | ||
| ENST00000564091.5:c.299C>A | ||
| ENST00000565140.5:c.1118C>A | ENSP00000455342.1:n.1118C>A | |
| ENST00000565316.5:c.1159C>A | ENSP00000456117.1:p.His387Asn | |
| ENST00000565354.5:n.523C>A | ||
| ENST00000566057.5:c.824C>A | ENSP00000456693.1:n.824C>A | |
| ENST00000567963.5:c.919C>A | ENSP00000455387.1:p.His307Asn | |
| ENST00000568076.5:n.1121C>A | ||
| ENST00000568224.4:c.976C>A | ENSP00000454253.1:p.His326Asn | |
| ENST00000568422.5:c.*447C>A | ENSP00000455549.1:n.*447C>A | |
| ENST00000568452.5:n.1338C>A | ||
| ENST00000569030.5:c.1002C>A | ENSP00000454680.1:n.1002C>A | |
| ENST00000569430.5:c.1210C>A | ENSP00000454229.1:p.His404Asn | |
| ENST00000628023.2:c.*506C>A | ENSP00000486178.1:n.*506C>A | |
| ENST00000631023.2:c.919C>A | ENSP00000486616.1:p.His307Asn | |
| NM_000086.2:c.1210C>A , LRG_689t1:c.1210C>A | NP_000077.1:p.His404Asn | |
| NM_001042432.1:c.1210C>A , LRG_689t2:c.1210C>A | NP_001035897.1:p.His404Asn | |
| NM_001286104.1:c.1138C>A | NP_001273033.1:p.His380Asn | |
| NM_001286105.1:c.910C>A | NP_001273034.1:p.His304Asn | |
| NM_001286109.1:c.976C>A | NP_001273038.1:p.His326Asn | |
| NM_001286110.1:c.1048C>A | NP_001273039.1:p.His350Asn | |
| NM_001042432.2:c.1210C>A MANE Select | NP_001035897.1:p.His404Asn | |
| NM_001286104.2:c.1138C>A | NP_001273033.1:p.His380Asn | |
| NM_001286105.2:c.910C>A | NP_001273034.1:p.His304Asn | |
| NM_001286109.2:c.976C>A | NP_001273038.1:p.His326Asn | |
| NM_001286110.2:c.1048C>A | NP_001273039.1:p.His350Asn |