HGVS | Genome Assembly |
---|---|
NC_000006.12:g.35805915G>A , CM000668.2:g.35805915G>A | GRCh38 |
NC_000006.11:g.35773692G>A , CM000668.1:g.35773692G>A | GRCh37 |
NC_000006.10:g.35881670G>A | NCBI36 |
NG_012184.1:g.5622G>A | |
NG_012184.2:g.5622G>A | |
NG_012184.3:g.13710G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360215.3:c.245G>A MANE Select | ENSP00000353346.1:p.Gly82Asp | |
ENST00000651132.1:c.245G>A | ENSP00000498322.1:p.Gly82Asp | |
ENST00000651676.1:c.245G>A | ENSP00000498699.1:p.Gly82Asp | |
ENST00000651994.1:c.245G>A | ENSP00000498310.1:p.Gly82Asp | |
ENST00000652718.1:c.77G>A | ENSP00000498866.1:p.Gly26Asp | |
ENST00000360215.2:c.245G>A | ENSP00000353346.1:p.Gly82Asp | |
NM_182548.3:c.245G>A | NP_872354.1:p.Gly82Asp | |
XM_011514403.1:c.245G>A | XP_011512705.1:p.Gly82Asp | |
NM_182548.4:c.245G>A MANE Select | NP_872354.1:p.Gly82Asp |