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