HGVS | Genome Assembly |
---|---|
NC_000006.12:g.55248639T>A , CM000668.2:g.55248639T>A | GRCh38 |
NC_000006.11:g.55113437T>A , CM000668.1:g.55113437T>A | GRCh37 |
NC_000006.10:g.55221396T>A | NCBI36 |
NG_012447.1:g.79367T>A | |
NG_012447.2:g.147180T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370862.4:c.224T>A MANE Select | ENSP00000359899.3:p.Val75Asp | |
ENST00000370862.3:c.224T>A | ENSP00000359899.3:p.Val75Asp | |
ENST00000615358.4:c.224T>A | ENSP00000477548.1:p.Val75Asp | |
NM_001526.3:c.224T>A | NP_001517.2:p.Val75Asp | |
XM_011514542.1:c.29T>A | XP_011512844.1:p.Val10Asp | |
NM_001526.4:c.224T>A | NP_001517.2:p.Val75Asp | |
XM_017010798.1:c.224T>A | XP_016866287.1:p.Val75Asp | |
NM_001384272.1:c.224T>A MANE Select | NP_001371201.1:p.Val75Asp | |
NM_001526.5:c.224T>A | NP_001517.2:p.Val75Asp |