HGVS | Genome Assembly |
---|---|
NC_000009.12:g.128345280A>G , CM000671.2:g.128345280A>G | GRCh38 |
NC_000009.11:g.131107559A>G , CM000671.1:g.131107559A>G | GRCh37 |
NC_000009.10:g.130147380A>G | NCBI36 |
NG_017057.1:g.9721A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000300456.5:c.287A>G MANE Select | ENSP00000300456.3:p.Glu96Gly | |
ENST00000300456.4:c.287A>G | ENSP00000300456.3:p.Glu96Gly | |
ENST00000372870.5:c.231+1999A>G | ENSP00000361961.1:n.231+1999A>G | |
NM_005094.3:c.287A>G | NP_005085.2:p.Glu96Gly | |
XM_017014222.1:c.287A>G | XP_016869711.1:p.Glu96Gly | |
XM_024447391.1:c.287A>G | XP_024303159.1:p.Glu96Gly | |
NM_005094.4:c.287A>G MANE Select | NP_005085.2:p.Glu96Gly |