Canonical Allele Identifier: CA2245897286
Gene: ATP1B2 HGNC NCBI

Linked Data

dbSNP Id: rs1597332844

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7648843A>G , CM000679.2:g.7648843A>G GRCh38
NC_000017.10:g.7552161A>G , CM000679.1:g.7552161A>G GRCh37
NC_000017.9:g.7492886A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577026.5:c.-6+2142A>G ENSP00000459145.1:n.-6+2142A>G
NM_001303263.1:c.-6+2142A>G NP_001290192.1:n.-6+2142A>G
NM_001303263.2:c.-6+2142A>G NP_001290192.1:n.-6+2142A>G