HGVS | Genome Assembly |
---|---|
NC_000017.11:g.74919538A>T , CM000679.2:g.74919538A>T | GRCh38 |
NC_000017.10:g.72915633A>T , CM000679.1:g.72915633A>T | GRCh37 |
NC_000017.9:g.70427228A>T | NCBI36 |
NG_007882.1:g.8719T>A | |
NG_033062.1:g.264A>T | |
NG_007882.2:g.8726T>A | |
NG_033062.2:g.264A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000614341.5:c.1298T>A MANE Select | ENSP00000480279.1:p.Leu433Gln | |
ENST00000579243.1:c.*897T>A | ENSP00000462568.1:n.*897T>A | |
ENST00000614341.4:c.1298T>A | ENSP00000480279.1:p.Leu433Gln | |
NM_001282489.2:c.989T>A | NP_001269418.1:p.Leu330Gln | |
NM_173477.4:c.1298T>A | NP_775748.2:p.Leu433Gln | |
XM_011524296.1:c.989T>A | XP_011522598.1:p.Leu330Gln | |
XM_011524296.2:c.989T>A | XP_011522598.1:p.Leu330Gln | |
NM_173477.5:c.1298T>A MANE Select | NP_775748.2:p.Leu433Gln | |
NM_001282489.3:c.989T>A | NP_001269418.1:p.Leu330Gln |