Canonical Allele Identifier: CA2635879639
Gene: ATP1B2 HGNC NCBI

Linked Data

gnomAD v4: 17-7654534-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7654534A>C , CM000679.2:g.7654534A>C GRCh38
NC_000017.10:g.7557852A>C , CM000679.1:g.7557852A>C GRCh37
NC_000017.9:g.7498577A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000250111.9:c.553-94A>C MANE Select ENSP00000250111.4:n.553-94A>C
ENST00000250111.8:c.553-94A>C ENSP00000250111.4:n.553-94A>C
ENST00000577026.5:c.307-94A>C ENSP00000459145.1:n.307-94A>C
ENST00000577113.1:c.150-94A>C
NM_001303263.1:c.307-94A>C NP_001290192.1:n.307-94A>C
NM_001678.4:c.553-94A>C NP_001669.3:n.553-94A>C
NM_001678.5:c.553-94A>C MANE Select NP_001669.3:n.553-94A>C
NM_001303263.2:c.307-94A>C NP_001290192.1:n.307-94A>C
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