Canonical Allele Identifier: CA421352843
Gene: ATP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs769240277
MyVariant Identifiers: chr1:g.160109773T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160139983T>G , CM000663.2:g.160139983T>G GRCh38
NC_000001.10:g.160109773T>G , CM000663.1:g.160109773T>G GRCh37
NC_000001.9:g.158376397T>G NCBI36
NG_008014.1:g.29226T>G , LRG_6:g.29226T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.3033T>G MANE Select ENSP00000354490.3:p.Gly1011=
ENST00000361216.7:c.3033T>G ENSP00000354490.3:p.Gly1011=
ENST00000392233.7:c.3000T>G ENSP00000376066.3:p.Gly1000=
ENST00000447527.1:c.2114T>G
ENST00000459972.1:n.25T>G
ENST00000463989.1:n.369T>G
NM_000702.3:c.3033T>G NP_000693.1:p.Gly1011=
NM_000702.4:c.3033T>G MANE Select NP_000693.1:p.Gly1011=
Search 100 bp 5'
Search 100 bp 3'