Linked Data
dbSNP Id:
rs267601965
ExAC:
8:65528704 G / A
gnomAD v2:
8-65528704-G-A
gnomAD v4:
8-64616147-G-A
COSMIC:
COSM4405121
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.64616147G>A , CM000670.2:g.64616147G>A | GRCh38 |
| NC_000008.10:g.65528704G>A , CM000670.1:g.65528704G>A | GRCh37 |
| NC_000008.9:g.65691258G>A | NCBI36 |
| NG_008338.1:g.187645C>T | |
| NG_008338.2:g.187645C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310193.4:c.394C>T MANE Select | ENSP00000310721.3:p.His132Tyr | |
| ENST00000310193.3:c.394C>T | ENSP00000310721.3:p.His132Tyr | |
| NM_004820.3:c.394C>T | NP_004811.1:p.His132Tyr | |
| NM_001324112.1:c.394C>T | NP_001311041.1:p.His132Tyr | |
| NM_004820.4:c.394C>T | NP_004811.1:p.His132Tyr | |
| XM_017014002.1:c.460C>T | XP_016869491.1:p.His154Tyr | |
| NM_004820.5:c.394C>T MANE Select | NP_004811.1:p.His132Tyr | |
| NM_001324112.2:c.394C>T | NP_001311041.1:p.His132Tyr |