dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.175443899A>C , CM000667.2:g.175443899A>C | GRCh38 |
| NC_000005.9:g.174870902A>C , CM000667.1:g.174870902A>C | GRCh37 |
| NC_000005.8:g.174803508A>C | NCBI36 |
| NG_011802.1:g.5262T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393752.3:c.-684T>G MANE Select | ENSP00000377353.1:n.-684T>G | |
| ENST00000393752.2:c.-684T>G | ENSP00000377353.1:n.-684T>G | |
| NM_000794.3:c.-684T>G | NP_000785.1:n.-684T>G | |
| NM_000794.4:c.-684T>G | NP_000785.1:n.-684T>G | |
| NM_000794.5:c.-684T>G MANE Select | NP_000785.1:n.-684T>G |