Canonical Allele Identifier: CA645917105
Gene: ATP1A2 HGNC NCBI

Linked Data

COSMIC: COSN24416059 COSN26949303
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160130619C>A , CM000663.2:g.160130619C>A GRCh38
NC_000001.10:g.160100409C>A , CM000663.1:g.160100409C>A GRCh37
NC_000001.9:g.158367033C>A NCBI36
NG_008014.1:g.19862C>A , LRG_6:g.19862C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.1827+22C>A MANE Select ENSP00000354490.3:n.1827+22C>A
ENST00000361216.7:c.1827+22C>A ENSP00000354490.3:n.1827+22C>A
ENST00000392233.7:c.1827+22C>A ENSP00000376066.3:n.1827+22C>A
ENST00000447527.1:c.959+22C>A
ENST00000472488.5:n.1930+22C>A
NM_000702.3:c.1827+22C>A NP_000693.1:n.1827+22C>A
NM_000702.4:c.1827+22C>A MANE Select NP_000693.1:n.1827+22C>A
Search 100 bp 5'
Search 100 bp 3'