Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.33005822C>G , CM000668.2:g.33005822C>G | GRCh38 |
| NC_000006.11:g.32973599C>G , CM000668.1:g.32973599C>G | GRCh37 |
| NC_000006.10:g.33081577C>G | NCBI36 |
| NG_012007.1:g.8791G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000229829.7:c.*1016G>C MANE Select | ENSP00000229829.3:n.*1016G>C | |
| ENST00000229829.6:c.*1016G>C | ENSP00000229829.3:n.*1016G>C | |
| NM_002119.3:c.*1016G>C | NP_002110.1:n.*1016G>C | |
| NM_002119.4:c.*1016G>C MANE Select | NP_002110.1:n.*1016G>C |