Canonical Allele Identifier: CA2245897282
Gene: ATP1B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7648839C= , CM000679.2:g.7648839C= GRCh38
NC_000017.10:g.7552157C= , CM000679.1:g.7552157C= GRCh37
NC_000017.9:g.7492882C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577026.5:c.-6+2138C= ENSP00000459145.1:n.-6+2138C=
NM_001303263.1:c.-6+2138C= NP_001290192.1:n.-6+2138C=
NM_001303263.2:c.-6+2138C= NP_001290192.1:n.-6+2138C=