Canonical Allele Identifier: CA2245900233

Gene: ATP1B2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7654527C= , CM000679.2:g.7654527C=	GRCh38
NC_000017.10:g.7557845C= , CM000679.1:g.7557845C=	GRCh37
NC_000017.9:g.7498570C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000250111.9:c.553-101C= MANE Select	ENSP00000250111.4:n.553-101C=
ENST00000250111.8:c.553-101C=	ENSP00000250111.4:n.553-101C=
ENST00000577026.5:c.307-101C=	ENSP00000459145.1:n.307-101C=
ENST00000577113.1:c.150-101C=
NM_001303263.1:c.307-101C=	NP_001290192.1:n.307-101C=
NM_001678.4:c.553-101C=	NP_001669.3:n.553-101C=
NM_001678.5:c.553-101C= MANE Select	NP_001669.3:n.553-101C=
NM_001303263.2:c.307-101C=	NP_001290192.1:n.307-101C=