HGVS | Genome Assembly |
---|---|
NC_000023.11:g.120626441T>A , CM000685.2:g.120626441T>A | GRCh38 |
NC_000023.10:g.119760296T>A , CM000685.1:g.119760296T>A | GRCh37 |
NC_000023.9:g.119644324T>A | NCBI36 |
NG_016219.1:g.8710A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000304661.6:c.726A>T MANE Select | ENSP00000304364.5:p.Gly242= | |
ENST00000304661.5:c.726A>T | ENSP00000304364.5:p.Gly242= | |
ENST00000371313.2:c.726A>T | ENSP00000360363.2:p.Gly242= | |
NM_001011551.2:c.726A>T | NP_001011551.1:p.Gly242= | |
NM_152692.4:c.726A>T | NP_689905.1:p.Gly242= | |
NM_001011551.3:c.726A>T MANE Select | NP_001011551.1:p.Gly242= | |
NM_152692.5:c.726A>T | NP_689905.1:p.Gly242= |