Canonical Allele Identifier: CA421600415
Gene: ATP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160105037A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160135247A>T , CM000663.2:g.160135247A>T GRCh38
NC_000001.10:g.160105037A>T , CM000663.1:g.160105037A>T GRCh37
NC_000001.9:g.158371661A>T NCBI36
NG_008014.1:g.24490A>T , LRG_6:g.24490A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361216.8:c.2067A>T MANE Select ENSP00000354490.3:p.Arg689=
ENST00000361216.7:c.2067A>T ENSP00000354490.3:p.Arg689=
ENST00000392233.7:c.2067A>T ENSP00000376066.3:p.Arg689=
ENST00000447527.1:c.1199A>T
ENST00000472488.5:n.2170A>T
NM_000702.3:c.2067A>T NP_000693.1:p.Arg689=
NM_000702.4:c.2067A>T MANE Select NP_000693.1:p.Arg689=
Search 100 bp 5'
Search 100 bp 3'