Linked Data
dbSNP Id:
rs767891880
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.192811799T>C , CM000663.2:g.192811799T>C | GRCh38 |
| NC_000001.10:g.192780929T>C , CM000663.1:g.192780929T>C | GRCh37 |
| NC_000001.9:g.191047552T>C | NCBI36 |
| NG_012800.1:g.7761T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000235382.7:c.*203T>C MANE Select | ENSP00000235382.5:n.*203T>C | |
| ENST00000235382.6:c.*203T>C | ENSP00000235382.5:n.*203T>C | |
| NM_002923.3:c.*203T>C | NP_002914.1:n.*203T>C | |
| NM_002923.4:c.*203T>C MANE Select | NP_002914.1:n.*203T>C |