HGVS | Genome Assembly |
---|---|
NC_000023.11:g.38408972G= , CM000685.2:g.38408972G= | GRCh38 |
NC_000023.10:g.38268225G= , CM000685.1:g.38268225G= | GRCh37 |
NC_000023.9:g.38153169G= | NCBI36 |
NG_008471.1:g.61490G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000039007.5:c.814G= MANE Select | ENSP00000039007.4:p.Glu272= | |
ENST00000643344.1:c.*564G= | ENSP00000496606.1:n.*564G= | |
ENST00000039007.4:c.814G= | ENSP00000039007.4:p.Glu272= | |
ENST00000465127.1:c.172-257149G= | ENSP00000417050.1:n.172-257149G= | |
NM_000531.5:c.814G= | NP_000522.3:p.Glu272= | |
XM_017029556.1:c.814G= | XP_016885045.1:p.Glu272= | |
NM_000531.6:c.814G= MANE Select | NP_000522.3:p.Glu272= |