dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33006624G>C , CM000668.2:g.33006624G>C | GRCh38 |
| NC_000006.11:g.32974401G>C , CM000668.1:g.32974401G>C | GRCh37 |
| NC_000006.10:g.33082379G>C | NCBI36 |
| NG_012007.1:g.7989C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000229829.7:c.*214C>G MANE Select | ENSP00000229829.3:n.*214C>G | |
| ENST00000229829.6:c.*214C>G | ENSP00000229829.3:n.*214C>G | |
| ENST00000490305.5:n.385C>G | ||
| NM_002119.3:c.*214C>G | NP_002110.1:n.*214C>G | |
| XM_005249047.3:c.*126C>G | XP_005249104.1:n.*126C>G | |
| XM_006715076.2:c.*214C>G | XP_006715139.1:n.*214C>G | |
| NM_002119.4:c.*214C>G MANE Select | NP_002110.1:n.*214C>G |