Canonical Allele Identifier: CA2245900240
Gene: ATP1B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7654531A= , CM000679.2:g.7654531A= GRCh38
NC_000017.10:g.7557849A= , CM000679.1:g.7557849A= GRCh37
NC_000017.9:g.7498574A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000250111.9:c.553-97A= MANE Select ENSP00000250111.4:n.553-97A=
ENST00000250111.8:c.553-97A= ENSP00000250111.4:n.553-97A=
ENST00000577026.5:c.307-97A= ENSP00000459145.1:n.307-97A=
ENST00000577113.1:c.150-97A=
NM_001303263.1:c.307-97A= NP_001290192.1:n.307-97A=
NM_001678.4:c.553-97A= NP_001669.3:n.553-97A=
NM_001678.5:c.553-97A= MANE Select NP_001669.3:n.553-97A=
NM_001303263.2:c.307-97A= NP_001290192.1:n.307-97A=
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