HGVS | Genome Assembly |
---|---|
NC_000004.12:g.42962917A>G , CM000666.2:g.42962917A>G | GRCh38 |
NC_000004.11:g.42964934A>G , CM000666.1:g.42964934A>G | GRCh37 |
NC_000004.10:g.42659691A>G | NCBI36 |
NG_027718.1:g.74652A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000399770.3:c.410A>G MANE Select | ENSP00000382670.2:p.Asp137Gly | |
ENST00000399770.2:c.410A>G | ENSP00000382670.2:p.Asp137Gly | |
NM_001080476.2:c.410A>G | NP_001073945.1:p.Asp137Gly | |
XM_011513691.1:c.47A>G | XP_011511993.1:p.Asp16Gly | |
NM_001080476.3:c.410A>G MANE Select | NP_001073945.1:p.Asp137Gly |