Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.112832722T= , CM000664.2:g.112832722T= | GRCh38 |
| NC_000002.11:g.113590299T= , CM000664.1:g.113590299T= | GRCh37 |
| NC_000002.10:g.113306770T= | NCBI36 |
| NG_008851.1:g.9058A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000263341.7:c.406A= MANE Select | ENSP00000263341.2:p.Met136= | |
| ENST00000263341.6:c.406A= | ENSP00000263341.2:p.Met136= | |
| ENST00000418817.5:c.406A= | ENSP00000407219.1:p.Met136= | |
| ENST00000487639.1:n.307A= | ||
| ENST00000491056.5:n.1213A= | ||
| NM_000576.2:c.406A= | NP_000567.1:p.Met136= | |
| XM_006712496.1:c.172A= | XP_006712559.1:p.Met58= | |
| XM_017003988.2:c.313A= | XP_016859477.1:p.Met105= | |
| NM_000576.3:c.406A= MANE Select | NP_000567.1:p.Met136= |