Canonical Allele Identifier: CA658795550
Gene: ATP1A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 529753
ClinVar RCV Id: RCV000635219
dbSNP Id: rs1553245152
MyVariant Identifiers: chr1:g.160100209T>C (hg19) chr1:g.160130419T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160130419T>C , CM000663.2:g.160130419T>C GRCh38
NC_000001.10:g.160100209T>C , CM000663.1:g.160100209T>C GRCh37
NC_000001.9:g.158366833T>C NCBI36
NG_008014.1:g.19662T>C , LRG_6:g.19662T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.1652-3T>C MANE Select ENSP00000354490.3:n.1652-3T>C
ENST00000361216.7:c.1652-3T>C ENSP00000354490.3:n.1652-3T>C
ENST00000392233.7:c.1652-3T>C ENSP00000376066.3:n.1652-3T>C
ENST00000447527.1:c.784-3T>C
ENST00000472488.5:n.1755-3T>C
NM_000702.3:c.1652-3T>C NP_000693.1:n.1652-3T>C
NM_000702.4:c.1652-3T>C MANE Select NP_000693.1:n.1652-3T>C
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