Canonical Allele Identifier: CA2245900241
Gene: ATP1B2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7654532G= , CM000679.2:g.7654532G= GRCh38
NC_000017.10:g.7557850G= , CM000679.1:g.7557850G= GRCh37
NC_000017.9:g.7498575G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000250111.9:c.553-96G= MANE Select ENSP00000250111.4:n.553-96G=
ENST00000250111.8:c.553-96G= ENSP00000250111.4:n.553-96G=
ENST00000577026.5:c.307-96G= ENSP00000459145.1:n.307-96G=
ENST00000577113.1:c.150-96G=
NM_001303263.1:c.307-96G= NP_001290192.1:n.307-96G=
NM_001678.4:c.553-96G= NP_001669.3:n.553-96G=
NM_001678.5:c.553-96G= MANE Select NP_001669.3:n.553-96G=
NM_001303263.2:c.307-96G= NP_001290192.1:n.307-96G=
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