Canonical Allele Identifier: CA343237073
Gene: ATP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1651625045

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160127579C>T , CM000663.2:g.160127579C>T GRCh38
NC_000001.10:g.160097369C>T , CM000663.1:g.160097369C>T GRCh37
NC_000001.9:g.158363993C>T NCBI36
NG_008014.1:g.16822C>T , LRG_6:g.16822C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.776C>T MANE Select ENSP00000354490.3:p.Thr259Ile
ENST00000361216.7:c.776C>T ENSP00000354490.3:p.Thr259Ile
ENST00000392233.7:c.776C>T ENSP00000376066.3:p.Thr259Ile
ENST00000472488.5:n.879C>T
NM_000702.3:c.776C>T NP_000693.1:p.Thr259Ile
NM_000702.4:c.776C>T MANE Select NP_000693.1:p.Thr259Ile