Canonical Allele Identifier: CA981202568
Gene: ATP1B2 HGNC NCBI

Linked Data

dbSNP Id: rs2072590874
gnomAD v3: 17-7648811-G-A
gnomAD v4: 17-7648811-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7648811G>A , CM000679.2:g.7648811G>A GRCh38
NC_000017.10:g.7552129G>A , CM000679.1:g.7552129G>A GRCh37
NC_000017.9:g.7492854G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577026.5:c.-6+2110G>A ENSP00000459145.1:n.-6+2110G>A
NM_001303263.1:c.-6+2110G>A NP_001290192.1:n.-6+2110G>A
NM_001303263.2:c.-6+2110G>A NP_001290192.1:n.-6+2110G>A