HGVS | Genome Assembly |
---|---|
NC_000011.10:g.640343G>A , CM000673.2:g.640343G>A | GRCh38 |
NC_000011.9:g.640343G>A , CM000673.1:g.640343G>A | GRCh37 |
NC_000011.8:g.630343G>A | NCBI36 |
NG_021241.1:g.8039G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000176183.6:c.1057+37G>A MANE Select | ENSP00000176183.5:n.1057+37G>A | |
ENST00000176183.5:c.1057+37G>A | ENSP00000176183.5:n.1057+37G>A | |
NM_000797.3:c.1057+37G>A | NP_000788.2:n.1057+37G>A | |
NM_000797.4:c.1057+37G>A MANE Select | NP_000788.2:n.1057+37G>A |