HGVS | Genome Assembly |
---|---|
NC_000013.11:g.110169653T>A , CM000675.2:g.110169653T>A | GRCh38 |
NC_000013.10:g.110822000T>A , CM000675.1:g.110822000T>A | GRCh37 |
NC_000013.9:g.109620001T>A | NCBI36 |
NG_011544.2:g.142497A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375820.10:c.3852A>T MANE Select | ENSP00000364979.4:p.Gly1284= | |
ENST00000650424.1:c.8A>T | ||
ENST00000375820.8:c.3852A>T | ENSP00000364979.4:p.Gly1284= | |
NM_001845.5:c.3852A>T | NP_001836.3:p.Gly1284= | |
XM_011521048.1:c.3660A>T | XP_011519350.1:p.Gly1220= | |
XM_011521048.2:c.3660A>T | XP_011519350.1:p.Gly1220= | |
NM_001845.6:c.3852A>T MANE Select | NP_001836.3:p.Gly1284= |