HGVS | Genome Assembly |
---|---|
NC_000022.11:g.43972242A>G , CM000684.2:g.43972242A>G | GRCh38 |
NC_000022.10:g.44368122A>G , CM000684.1:g.44368122A>G | GRCh37 |
NC_000022.9:g.42699455A>G | NCBI36 |
NG_029057.1:g.21862A>G | |
NG_029057.2:g.21862A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000350028.5:c.329A>G MANE Select | ENSP00000345445.4:p.Asp110Gly | |
ENST00000350028.4:c.329A>G | ENSP00000345445.4:p.Asp110Gly | |
ENST00000493161.1:n.511A>G | ||
NM_015380.4:c.329A>G | NP_056195.3:p.Asp110Gly | |
NM_015380.5:c.329A>G MANE Select | NP_056195.3:p.Asp110Gly |