HGVS | Genome Assembly |
---|---|
NC_000011.10:g.69648054T>G , CM000673.2:g.69648054T>G | GRCh38 |
NC_000011.9:g.69462822T>G , CM000673.1:g.69462822T>G | GRCh37 |
NC_000011.8:g.69172003T>G | NCBI36 |
NG_007375.1:g.11950T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000227507.3:c.635T>G MANE Select | ENSP00000227507.2:p.Val212Gly | |
ENST00000227507.2:c.635T>G | ENSP00000227507.2:p.Val212Gly | |
ENST00000536559.1:c.*55T>G | ENSP00000438482.1:n.*55T>G | |
ENST00000542367.1:n.98T>G | ||
ENST00000545484.1:n.341T>G | ||
NM_053056.2:c.635T>G | NP_444284.1:p.Val212Gly | |
XM_006718653.2:c.659T>G | XP_006718716.1:p.Val220Gly | |
NM_053056.3:c.635T>G MANE Select | NP_444284.1:p.Val212Gly |