Linked Data
ClinVar Variation Id:
1401302
dbSNP Id:
rs368236000
ExAC:
4:6303405 C / T
gnomAD v2:
4-6303405-C-T
gnomAD v3:
4-6301678-C-T
gnomAD v4:
4-6301678-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.6301678C>T , CM000666.2:g.6301678C>T | GRCh38 |
| NC_000004.11:g.6303405C>T , CM000666.1:g.6303405C>T | GRCh37 |
| NC_000004.10:g.6354306C>T | NCBI36 |
| NG_011700.1:g.36829C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682275.1:c.1919C>T | ENSP00000507852.1:p.Thr640Met | |
| ENST00000683395.1:c.1860C>T | ||
| ENST00000684087.1:c.1883C>T | ENSP00000506978.1:p.Thr628Met | |
| ENST00000506362.2:c.1634C>T | ENSP00000424103.2:p.Thr545Met | |
| ENST00000673642.1:c.1542C>T | ENSP00000501242.1:n.1542C>T | |
| ENST00000673991.1:c.1919C>T | ENSP00000501033.1:p.Thr640Met | |
| ENST00000226760.5:c.1883C>T MANE Select | ENSP00000226760.1:p.Thr628Met | |
| ENST00000503569.5:c.1883C>T | ENSP00000423337.1:p.Thr628Met | |
| ENST00000507765.1:n.2068C>T | ||
| NM_001145853.1:c.1883C>T | NP_001139325.1:p.Thr628Met | |
| NM_006005.3:c.1883C>T MANE Select | NP_005996.2:p.Thr628Met | |
| XM_017008586.1:c.1892C>T | XP_016864075.1:p.Thr631Met |