Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240875203A= , CM000664.2:g.240875203A= | GRCh38 |
| NC_000002.11:g.241814620A= , CM000664.1:g.241814620A= | GRCh37 |
| NC_000002.10:g.241463293A= | NCBI36 |
| NG_008005.1:g.11459A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.775A= MANE Select | ENSP00000302620.3:p.Met259= | |
| ENST00000307503.3:c.775A= | ENSP00000302620.3:p.Met259= | |
| ENST00000476698.1:n.427A= | ||
| NM_000030.2:c.775A= | NP_000021.1:p.Met259= | |
| NM_000030.3:c.775A= MANE Select | NP_000021.1:p.Met259= |