HGVS | Genome Assembly |
---|---|
NC_000020.11:g.46010947C= , CM000682.2:g.46010947C= | GRCh38 |
NC_000020.10:g.44639586C= , CM000682.1:g.44639586C= | GRCh37 |
NC_000020.9:g.44072993C= | NCBI36 |
NG_011468.1:g.7040C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372330.3:c.546C= MANE Select | ENSP00000361405.3:p.Asp182= | |
NM_004994.2:c.546C= | NP_004985.2:p.Asp182= | |
NM_004994.3:c.546C= MANE Select | NP_004985.2:p.Asp182= |