HGVS | Genome Assembly |
---|---|
NC_000023.11:g.38401343C>G , CM000685.2:g.38401343C>G | GRCh38 |
NC_000023.10:g.38260596C>G , CM000685.1:g.38260596C>G | GRCh37 |
NC_000023.9:g.38145540C>G | NCBI36 |
NG_008471.1:g.53861C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000039007.5:c.455C>G MANE Select | ENSP00000039007.4:p.Ala152Gly | |
ENST00000643344.1:c.*205C>G | ENSP00000496606.1:n.*205C>G | |
ENST00000039007.4:c.455C>G | ENSP00000039007.4:p.Ala152Gly | |
ENST00000465127.1:c.172-264778C>G | ENSP00000417050.1:n.172-264778C>G | |
ENST00000488812.1:n.492C>G | ||
NM_000531.5:c.455C>G | NP_000522.3:p.Ala152Gly | |
XM_017029556.1:c.455C>G | XP_016885045.1:p.Ala152Gly | |
NM_000531.6:c.455C>G MANE Select | NP_000522.3:p.Ala152Gly |