Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31266861T= , CM000664.2:g.31266861T= | GRCh38 |
| NC_000002.11:g.31489727T= , CM000664.1:g.31489727T= | GRCh37 |
| NC_000002.10:g.31343231T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000322054.10:c.*157T= MANE Select | ENSP00000327116.5:n.*157T= | |
| ENST00000322054.9:c.*157T= | ENSP00000327116.5:n.*157T= | |
| ENST00000541626.2:c.*123T= | ENSP00000440685.2:n.*123T= | |
| NM_014600.2:c.*157T= | NP_055415.1:n.*157T= | |
| XM_011532806.1:c.*157T= | XP_011531108.1:n.*157T= | |
| XM_011532806.2:c.*157T= | XP_011531108.1:n.*157T= | |
| NM_014600.3:c.*157T= MANE Select | NP_055415.1:n.*157T= |