Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29062385C= , CM000664.2:g.29062385C= | GRCh38 |
| NC_000002.11:g.29285251C= , CM000664.1:g.29285251C= | GRCh37 |
| NC_000002.10:g.29138755C= | NCBI36 |
| NG_021427.1:g.16877G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331664.6:c.*2484G= MANE Select | ENSP00000332809.4:n.*2484G= | |
| ENST00000331664.5:c.6351G= | ENSP00000332809.4:n.6351G= | |
| NM_001029883.2:c.6351G= | NP_001025054.1:n.6351G= | |
| XM_011532826.1:c.*382-730G= | XP_011531128.1:n.*382-730G= | |
| NM_001029883.3:c.*2484G= MANE Select | NP_001025054.1:n.*2484G= |