Canonical Allele Identifier: CA775158957

Gene: ATP1B2

Linked Data

• dbSNP Id: rs1230883560
• MyVariant Identifiers: chr17:g.7557837C>T (hg19) ; chr17:g.7654519C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7654519C>T , CM000679.2:g.7654519C>T	GRCh38
NC_000017.10:g.7557837C>T , CM000679.1:g.7557837C>T	GRCh37
NC_000017.9:g.7498562C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000250111.9:c.553-109C>T MANE Select	ENSP00000250111.4:n.553-109C>T
ENST00000250111.8:c.553-109C>T	ENSP00000250111.4:n.553-109C>T
ENST00000577026.5:c.307-109C>T	ENSP00000459145.1:n.307-109C>T
ENST00000577113.1:c.150-109C>T
NM_001303263.1:c.307-109C>T	NP_001290192.1:n.307-109C>T
NM_001678.4:c.553-109C>T	NP_001669.3:n.553-109C>T
NM_001678.5:c.553-109C>T MANE Select	NP_001669.3:n.553-109C>T
NM_001303263.2:c.307-109C>T	NP_001290192.1:n.307-109C>T