Canonical Allele Identifier: CA1202191846
Gene: ATP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160127570T= , CM000663.2:g.160127570T= GRCh38
NC_000001.10:g.160097360T= , CM000663.1:g.160097360T= GRCh37
NC_000001.9:g.158363984T= NCBI36
NG_008014.1:g.16813T= , LRG_6:g.16813T=

Transcript Alleles

HGVS Amino-acid change
ENST00000361216.8:c.767T= MANE Select ENSP00000354490.3:p.Val256=
ENST00000361216.7:c.767T= ENSP00000354490.3:p.Val256=
ENST00000392233.7:c.767T= ENSP00000376066.3:p.Val256=
ENST00000472488.5:n.870T=
NM_000702.3:c.767T= NP_000693.1:p.Val256=
NM_000702.4:c.767T= MANE Select NP_000693.1:p.Val256=