Canonical Allele Identifier: CA2245897269
Gene: ATP1B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7648812G= , CM000679.2:g.7648812G= GRCh38
NC_000017.10:g.7552130G= , CM000679.1:g.7552130G= GRCh37
NC_000017.9:g.7492855G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000577026.5:c.-6+2111G= ENSP00000459145.1:n.-6+2111G=
NM_001303263.1:c.-6+2111G= NP_001290192.1:n.-6+2111G=
NM_001303263.2:c.-6+2111G= NP_001290192.1:n.-6+2111G=