Canonical Allele Identifier: CA31505783
Gene: ATP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs954630925
MyVariant Identifiers: chr1:g.160109153T>C (hg19) chr1:g.160139363T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160139363T>C , CM000663.2:g.160139363T>C GRCh38
NC_000001.10:g.160109153T>C , CM000663.1:g.160109153T>C GRCh37
NC_000001.9:g.158375777T>C NCBI36
NG_008014.1:g.28606T>C , LRG_6:g.28606T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.2841-277T>C MANE Select ENSP00000354490.3:n.2841-277T>C
ENST00000361216.7:c.2841-277T>C ENSP00000354490.3:n.2841-277T>C
ENST00000392233.7:c.2841-277T>C ENSP00000376066.3:n.2841-277T>C
ENST00000447527.1:c.1922-277T>C
ENST00000463989.1:n.177-277T>C
NM_000702.3:c.2841-277T>C NP_000693.1:n.2841-277T>C
NM_000702.4:c.2841-277T>C MANE Select NP_000693.1:n.2841-277T>C
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