HGVS | Genome Assembly |
---|---|
NC_000011.10:g.69648045T>G , CM000673.2:g.69648045T>G | GRCh38 |
NC_000011.9:g.69462813T>G , CM000673.1:g.69462813T>G | GRCh37 |
NC_000011.8:g.69171994T>G | NCBI36 |
NG_007375.1:g.11941T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000227507.3:c.626T>G MANE Select | ENSP00000227507.2:p.Val209Gly | |
ENST00000227507.2:c.626T>G | ENSP00000227507.2:p.Val209Gly | |
ENST00000536559.1:c.*46T>G | ENSP00000438482.1:n.*46T>G | |
ENST00000542367.1:n.89T>G | ||
ENST00000545484.1:n.332T>G | ||
NM_053056.2:c.626T>G | NP_444284.1:p.Val209Gly | |
XM_006718653.2:c.650T>G | XP_006718716.1:p.Val217Gly | |
NM_053056.3:c.626T>G MANE Select | NP_444284.1:p.Val209Gly |