Canonical Allele Identifier: CA2245897294
Gene: ATP1B2 HGNC NCBI

Linked Data

dbSNP Id: rs1597332852

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7648850T>C , CM000679.2:g.7648850T>C GRCh38
NC_000017.10:g.7552168T>C , CM000679.1:g.7552168T>C GRCh37
NC_000017.9:g.7492893T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577026.5:c.-6+2149T>C ENSP00000459145.1:n.-6+2149T>C
NM_001303263.1:c.-6+2149T>C NP_001290192.1:n.-6+2149T>C
NM_001303263.2:c.-6+2149T>C NP_001290192.1:n.-6+2149T>C