Canonical Allele Identifier: CA2245897300
Gene: ATP1B2 HGNC NCBI

Linked Data

dbSNP Id: rs967933295
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7648855A>C , CM000679.2:g.7648855A>C GRCh38
NC_000017.10:g.7552173A>C , CM000679.1:g.7552173A>C GRCh37
NC_000017.9:g.7492898A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000577026.5:c.-6+2154A>C ENSP00000459145.1:n.-6+2154A>C
NM_001303263.1:c.-6+2154A>C NP_001290192.1:n.-6+2154A>C
NM_001303263.2:c.-6+2154A>C NP_001290192.1:n.-6+2154A>C
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