Canonical Allele Identifier: CA421599388
Gene: ATP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160097355C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160127565C>G , CM000663.2:g.160127565C>G GRCh38
NC_000001.10:g.160097355C>G , CM000663.1:g.160097355C>G GRCh37
NC_000001.9:g.158363979C>G NCBI36
NG_008014.1:g.16808C>G , LRG_6:g.16808C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361216.8:c.762C>G MANE Select ENSP00000354490.3:p.Gly254=
ENST00000361216.7:c.762C>G ENSP00000354490.3:p.Gly254=
ENST00000392233.7:c.762C>G ENSP00000376066.3:p.Gly254=
ENST00000472488.5:n.865C>G
NM_000702.3:c.762C>G NP_000693.1:p.Gly254=
NM_000702.4:c.762C>G MANE Select NP_000693.1:p.Gly254=
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Search 100 bp 3'