HGVS | Genome Assembly |
---|---|
NC_000023.11:g.48527248T>G , CM000685.2:g.48527248T>G | GRCh38 |
NC_000023.10:g.48385636T>G , CM000685.1:g.48385636T>G | GRCh37 |
NC_000023.9:g.48270580T>G | NCBI36 |
NG_007452.1:g.10473T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000495186.6:c.432T>G MANE Select | ENSP00000417052.1:p.His144Gln | |
ENST00000651615.1:c.432T>G | ENSP00000498524.1:p.His144Gln | |
ENST00000276096.10:n.390T>G | ||
ENST00000414061.1:c.432T>G | ENSP00000405832.1:p.His144Gln | |
ENST00000446158.5:c.432T>G | ENSP00000390031.1:p.His144Gln | |
ENST00000466461.1:n.271T>G | ||
ENST00000495186.5:c.432T>G | ENSP00000417052.1:p.His144Gln | |
ENST00000498425.1:n.553T>G | ||
NM_006579.2:c.432T>G | NP_006570.1:p.His144Gln | |
NM_006579.3:c.432T>G MANE Select | NP_006570.1:p.His144Gln |