HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73322703C>A , CM000677.2:g.73322703C>A | GRCh38 |
NC_000015.9:g.73615044C>A , CM000677.1:g.73615044C>A | GRCh37 |
NC_000015.8:g.71402097C>A | NCBI36 |
NG_009063.1:g.51562G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.3390G>T MANE Select | ENSP00000261917.3:p.Gly1130= | |
ENST00000261917.3:c.3390G>T | ENSP00000261917.3:p.Gly1130= | |
NM_005477.2:c.3390G>T | NP_005468.1:p.Gly1130= | |
XM_011521148.1:c.2172G>T | XP_011519450.1:p.Gly724= | |
XM_011521148.2:c.2172G>T | XP_011519450.1:p.Gly724= | |
NM_005477.3:c.3390G>T MANE Select | NP_005468.1:p.Gly1130= |