Canonical Allele Identifier: CA775164051

Gene: ATP1B2

Linked Data

• dbSNP Id: rs1176018588
• MyVariant Identifiers: chr17:g.7552128A>G (hg19) ; chr17:g.7648810A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7648810A>G , CM000679.2:g.7648810A>G	GRCh38
NC_000017.10:g.7552128A>G , CM000679.1:g.7552128A>G	GRCh37
NC_000017.9:g.7492853A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577026.5:c.-6+2109A>G	ENSP00000459145.1:n.-6+2109A>G
NM_001303263.1:c.-6+2109A>G	NP_001290192.1:n.-6+2109A>G
NM_001303263.2:c.-6+2109A>G	NP_001290192.1:n.-6+2109A>G