Canonical Allele Identifier: CA2808382988

Gene: ATP1B2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7648817A>T , CM000679.2:g.7648817A>T	GRCh38
NC_000017.10:g.7552135A>T , CM000679.1:g.7552135A>T	GRCh37
NC_000017.9:g.7492860A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000577026.5:c.-6+2116A>T	ENSP00000459145.1:n.-6+2116A>T
NM_001303263.1:c.-6+2116A>T	NP_001290192.1:n.-6+2116A>T
NM_001303263.2:c.-6+2116A>T	NP_001290192.1:n.-6+2116A>T