Linked Data
dbSNP Id:
rs9273437
gnomAD v2:
6-32627522-C-T
gnomAD v3:
6-32659745-C-T
gnomAD v4:
6-32659745-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32659745C>T , CM000668.2:g.32659745C>T | GRCh38 |
| NC_000006.11:g.32627522C>T , CM000668.1:g.32627522C>T | GRCh37 |
| NC_000006.10:g.32735500C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000434651.7:c.*491G>A MANE Select | ENSP00000407332.2:n.*491G>A | |
| ENST00000374943.8:c.*491G>A | ENSP00000364080.4:n.*491G>A | |
| ENST00000399079.7:c.*491G>A | ENSP00000382029.3:n.*491G>A | |
| ENST00000399082.7:c.*491G>A | ENSP00000382032.3:n.*491G>A | |
| ENST00000399084.5:c.*491G>A | ENSP00000382034.1:n.*491G>A | |
| ENST00000434651.6:c.*491G>A | ENSP00000407332.2:n.*491G>A | |
| ENST00000487676.1:n.4366G>A | ||
| NM_001243961.1:c.*491G>A | NP_001230890.1:n.*491G>A | |
| NM_002123.4:c.*491G>A | NP_002114.3:n.*491G>A | |
| NM_001243961.2:c.*491G>A | NP_001230890.1:n.*491G>A | |
| NM_002123.5:c.*491G>A MANE Select | NP_002114.3:n.*491G>A |