Canonical Allele Identifier: CA421351021
Gene: ATP1A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1116845
ClinVar RCV Id: RCV001445390
dbSNP Id: rs2101990844
MyVariant Identifiers: chr1:g.160100384C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160130594C>A , CM000663.2:g.160130594C>A GRCh38
NC_000001.10:g.160100384C>A , CM000663.1:g.160100384C>A GRCh37
NC_000001.9:g.158367008C>A NCBI36
NG_008014.1:g.19837C>A , LRG_6:g.19837C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.1824C>A MANE Select ENSP00000354490.3:p.Ile608=
ENST00000361216.7:c.1824C>A ENSP00000354490.3:p.Ile608=
ENST00000392233.7:c.1824C>A ENSP00000376066.3:p.Ile608=
ENST00000447527.1:c.956C>A
ENST00000472488.5:n.1927C>A
NM_000702.3:c.1824C>A NP_000693.1:p.Ile608=
NM_000702.4:c.1824C>A MANE Select NP_000693.1:p.Ile608=
Search 100 bp 5'
Search 100 bp 3'