HGVS | Genome Assembly |
---|---|
NC_000012.12:g.49950966A= , CM000674.2:g.49950966A= | GRCh38 |
NC_000012.11:g.50344749A= , CM000674.1:g.50344749A= | GRCh37 |
NC_000012.10:g.48631016A= | NCBI36 |
NG_008913.1:g.5226A= , LRG_717:g.5226A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000199280.4:c.136A= MANE Select | ENSP00000199280.3:p.Met46= | |
ENST00000199280.3:c.136A= | ENSP00000199280.3:p.Met46= | |
ENST00000550862.1:c.136A= | ENSP00000450022.1:p.Met46= | |
ENST00000551526.5:c.136A= | ENSP00000447148.1:p.Met46= | |
NM_000486.5:c.136A= , LRG_717t1:c.136A= | NP_000477.1:p.Met46= | |
NM_000486.6:c.136A= MANE Select | NP_000477.1:p.Met46= |