Linked Data
ClinVar Variation Id:
135698
dbSNP Id:
rs145181563
ExAC:
5:112174919 C / T
gnomAD v2:
5-112174919-C-T
gnomAD v3:
5-112839222-C-T
gnomAD v4:
5-112839222-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112839222C>T , CM000667.2:g.112839222C>T | GRCh38 |
| NC_000005.9:g.112174919C>T , CM000667.1:g.112174919C>T | GRCh37 |
| NC_000005.8:g.112202818C>T | NCBI36 |
| NG_008481.4:g.151702C>T , LRG_130:g.151702C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.3293C>T | ENSP00000484935.2:n.3293C>T | |
| ENST00000504915.3:c.3682C>T | ENSP00000473355.2:p.His1228Tyr | |
| ENST00000505350.2:c.*3634C>T | ENSP00000481752.1:n.*3634C>T | |
| ENST00000507379.6:c.3574C>T | ENSP00000423224.2:p.His1192Tyr | |
| ENST00000509732.6:c.3628C>T | ENSP00000426541.2:p.His1210Tyr | |
| ENST00000512211.7:c.3628C>T | ENSP00000423828.3:p.His1210Tyr | |
| ENST00000257430.9:c.3628C>T MANE Select | ENSP00000257430.4:p.His1210Tyr | |
| ENST00000257430.8:c.3628C>T | ENSP00000257430.4:p.His1210Tyr | |
| ENST00000502371.2:c.1981C>T | ||
| ENST00000508376.6:c.3628C>T | ENSP00000427089.2:p.His1210Tyr | |
| ENST00000508624.5:c.*2950C>T | ENSP00000424265.1:n.*2950C>T | |
| ENST00000512211.6:c.3628C>T | ENSP00000423828.2:p.His1210Tyr | |
| ENST00000520401.1:c.230+10250C>T | ||
| NM_000038.5:c.3628C>T | NP_000029.2:p.His1210Tyr | |
| NM_001127510.2:c.3628C>T | NP_001120982.1:p.His1210Tyr | |
| NM_001127511.2:c.3574C>T | NP_001120983.2:p.His1192Tyr | |
| NM_001354895.1:c.3628C>T | NP_001341824.1:p.His1210Tyr | |
| NM_001354896.1:c.3682C>T | NP_001341825.1:p.His1228Tyr | |
| NM_001354897.1:c.3658C>T | NP_001341826.1:p.His1220Tyr | |
| NM_001354898.1:c.3553C>T | NP_001341827.1:p.His1185Tyr | |
| NM_001354899.1:c.3544C>T | NP_001341828.1:p.His1182Tyr | |
| NM_001354900.1:c.3505C>T | NP_001341829.1:p.His1169Tyr | |
| NM_001354901.1:c.3451C>T | NP_001341830.1:p.His1151Tyr | |
| NM_001354902.1:c.3355C>T | NP_001341831.1:p.His1119Tyr | |
| NM_001354903.1:c.3325C>T | NP_001341832.1:p.His1109Tyr | |
| NM_001354904.1:c.3250C>T | NP_001341833.1:p.His1084Tyr | |
| NM_001354905.1:c.3148C>T | NP_001341834.1:p.His1050Tyr | |
| NM_001354906.1:c.2779C>T | NP_001341835.1:p.His927Tyr | |
| NM_000038.6:c.3628C>T MANE Select | NP_000029.2:p.His1210Tyr | |
| NM_001127510.3:c.3628C>T | NP_001120982.1:p.His1210Tyr | |
| NM_001127511.3:c.3574C>T | NP_001120983.2:p.His1192Tyr | |
| NM_001354895.2:c.3628C>T | NP_001341824.1:p.His1210Tyr | |
| NM_001354896.2:c.3682C>T | NP_001341825.1:p.His1228Tyr | |
| NM_001354897.2:c.3658C>T | NP_001341826.1:p.His1220Tyr | |
| NM_001354898.2:c.3553C>T | NP_001341827.1:p.His1185Tyr | |
| NM_001354899.2:c.3544C>T | NP_001341828.1:p.His1182Tyr | |
| NM_001354900.2:c.3505C>T | NP_001341829.1:p.His1169Tyr | |
| NM_001354901.2:c.3451C>T | NP_001341830.1:p.His1151Tyr | |
| NM_001354902.2:c.3355C>T | NP_001341831.1:p.His1119Tyr | |
| NM_001354903.2:c.3325C>T | NP_001341832.1:p.His1109Tyr | |
| NM_001354904.2:c.3250C>T | NP_001341833.1:p.His1084Tyr | |
| NM_001354905.2:c.3148C>T | NP_001341834.1:p.His1050Tyr | |
| NM_001354906.2:c.2779C>T | NP_001341835.1:p.His927Tyr |