Canonical Allele Identifier: CA343243803
Gene: ATP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160100076T>G (hg19) chr1:g.160130286T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160130286T>G , CM000663.2:g.160130286T>G GRCh38
NC_000001.10:g.160100076T>G , CM000663.1:g.160100076T>G GRCh37
NC_000001.9:g.158366700T>G NCBI36
NG_008014.1:g.19529T>G , LRG_6:g.19529T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361216.8:c.1646T>G MANE Select ENSP00000354490.3:p.Val549Gly
ENST00000361216.7:c.1646T>G ENSP00000354490.3:p.Val549Gly
ENST00000392233.7:c.1646T>G ENSP00000376066.3:p.Val549Gly
ENST00000447527.1:c.778T>G
ENST00000472488.5:n.1749T>G
NM_000702.3:c.1646T>G NP_000693.1:p.Val549Gly
NM_000702.4:c.1646T>G MANE Select NP_000693.1:p.Val549Gly
Search 100 bp 5'
Search 100 bp 3'