Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29062377A= , CM000664.2:g.29062377A= | GRCh38 |
| NC_000002.11:g.29285243A= , CM000664.1:g.29285243A= | GRCh37 |
| NC_000002.10:g.29138747A= | NCBI36 |
| NG_021427.1:g.16885T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331664.6:c.*2492T= MANE Select | ENSP00000332809.4:n.*2492T= | |
| ENST00000331664.5:c.6359T= | ENSP00000332809.4:n.6359T= | |
| NM_001029883.2:c.6359T= | NP_001025054.1:n.6359T= | |
| XM_011532826.1:c.*382-722T= | XP_011531128.1:n.*382-722T= | |
| NM_001029883.3:c.*2492T= MANE Select | NP_001025054.1:n.*2492T= |