Canonical Allele Identifier: CA526678392
Gene: ATP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1386994782
gnomAD v2: 1-160097300-G-A
gnomAD v4: 1-160127510-G-A
MyVariant Identifiers: chr1:g.160097300G>A (hg19) chr1:g.160127510G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160127510G>A , CM000663.2:g.160127510G>A GRCh38
NC_000001.10:g.160097300G>A , CM000663.1:g.160097300G>A GRCh37
NC_000001.9:g.158363924G>A NCBI36
NG_008014.1:g.16753G>A , LRG_6:g.16753G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.749-42G>A MANE Select ENSP00000354490.3:n.749-42G>A
ENST00000361216.7:c.749-42G>A ENSP00000354490.3:n.749-42G>A
ENST00000392233.7:c.749-42G>A ENSP00000376066.3:n.749-42G>A
ENST00000472488.5:n.852-42G>A
NM_000702.3:c.749-42G>A NP_000693.1:n.749-42G>A
NM_000702.4:c.749-42G>A MANE Select NP_000693.1:n.749-42G>A
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