Linked Data
ClinVar Variation Id:
55447
dbSNP Id:
rs80357171
ExAC:
17:41215354 T / C
gnomAD v2:
17-41215354-T-C
gnomAD v3:
17-43063337-T-C
gnomAD v4:
17-43063337-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43063337T>C , CM000679.2:g.43063337T>C | GRCh38 |
| NC_000017.10:g.41215354T>C , CM000679.1:g.41215354T>C | GRCh37 |
| NC_000017.9:g.38468880T>C | NCBI36 |
| NG_005905.2:g.154647A>G , LRG_292:g.154647A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461574.2:c.5186A>G | ENSP00000417241.2:p.Asn1729Ser | |
| ENST00000470026.6:c.5189A>G | ENSP00000419274.2:p.Asn1730Ser | |
| ENST00000473961.6:c.5063A>G | ENSP00000420201.2:p.Asn1688Ser | |
| ENST00000476777.6:c.5183A>G | ENSP00000417554.2:p.Asn1728Ser | |
| ENST00000477152.6:c.5111A>G | ENSP00000419988.2:p.Asn1704Ser | |
| ENST00000478531.6:c.1877A>G | ENSP00000420412.2:p.Asn626Ser | |
| ENST00000489037.2:c.5111A>G | ENSP00000420781.2:p.Asn1704Ser | |
| ENST00000493919.6:c.1739A>G | ENSP00000418819.2:p.Asn580Ser | |
| ENST00000494123.6:c.5189A>G | ENSP00000419103.2:p.Asn1730Ser | |
| ENST00000497488.2:c.4301A>G | ENSP00000418986.2:p.Asn1434Ser | |
| ENST00000618469.2:c.5189A>G | ENSP00000478114.2:p.Asn1730Ser | |
| ENST00000634433.2:c.5066A>G | ENSP00000489431.2:p.Asn1689Ser | |
| ENST00000644379.2:c.5255A>G | ENSP00000496570.2:p.Asn1752Ser | |
| ENST00000644555.2:c.1739A>G | ENSP00000494614.2:p.Asn580Ser | |
| ENST00000652672.2:c.5048A>G | ENSP00000498906.2:p.Asn1683Ser | |
| ENST00000484087.6:c.1751A>G | ENSP00000419481.2:p.Asn584Ser | |
| ENST00000357654.9:c.5189A>G MANE Select | ENSP00000350283.3:p.Asn1730Ser | |
| ENST00000471181.7:c.5252A>G | ENSP00000418960.2:p.Asn1751Ser | |
| ENST00000644379.1:c.1576A>G | ||
| ENST00000352993.7:c.1763A>G | ENSP00000312236.5:p.Asn588Ser | |
| ENST00000357654.7:c.5189A>G | ENSP00000350283.3:p.Asn1730Ser | |
| ENST00000461221.5:c.*4972A>G | ENSP00000418548.1:n.*4972A>G | |
| ENST00000468300.5:c.1877A>G | ENSP00000417148.1:p.Asn626Ser | |
| ENST00000471181.6:c.5252A>G | ENSP00000418960.2:p.Asn1751Ser | |
| ENST00000491747.6:c.1877A>G | ENSP00000420705.2:p.Asn626Ser | |
| ENST00000493795.5:c.5048A>G | ENSP00000418775.1:p.Asn1683Ser | |
| ENST00000586385.5:c.119A>G | ENSP00000465818.1:p.Asn40Ser | |
| ENST00000591534.5:c.662A>G | ENSP00000467329.1:p.Asn221Ser | |
| ENST00000591849.5:c.-98-13147A>G | ENSP00000465347.1:n.-98-13147A>G | |
| NM_007294.3:c.5189A>G , LRG_292t1:c.5189A>G | NP_009225.1:p.Asn1730Ser | |
| NM_007297.3:c.5048A>G | NP_009228.2:p.Asn1683Ser | |
| NM_007298.3:c.1877A>G | NP_009229.2:p.Asn626Ser | |
| NM_007299.3:c.1877A>G | NP_009230.2:p.Asn626Ser | |
| NM_007300.3:c.5252A>G | NP_009231.2:p.Asn1751Ser | |
| NR_027676.1:n.5325A>G | ||
| NM_007294.4:c.5189A>G MANE Select | NP_009225.1:p.Asn1730Ser | |
| NM_007297.4:c.5048A>G | NP_009228.2:p.Asn1683Ser | |
| NM_007299.4:c.1877A>G | NP_009230.2:p.Asn626Ser | |
| NM_007300.4:c.5252A>G | NP_009231.2:p.Asn1751Ser | |
| NR_027676.2:n.5366A>G |