Canonical Allele Identifier: CA421600364
Gene: ATP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160100077G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160130287G>C , CM000663.2:g.160130287G>C GRCh38
NC_000001.10:g.160100077G>C , CM000663.1:g.160100077G>C GRCh37
NC_000001.9:g.158366701G>C NCBI36
NG_008014.1:g.19530G>C , LRG_6:g.19530G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000361216.8:c.1647G>C MANE Select ENSP00000354490.3:p.Val549=
ENST00000361216.7:c.1647G>C ENSP00000354490.3:p.Val549=
ENST00000392233.7:c.1647G>C ENSP00000376066.3:p.Val549=
ENST00000447527.1:c.779G>C
ENST00000472488.5:n.1750G>C
NM_000702.3:c.1647G>C NP_000693.1:p.Val549=
NM_000702.4:c.1647G>C MANE Select NP_000693.1:p.Val549=
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