Canonical Allele Identifier: CA2245900230
Gene: ATP1B2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7654517G= , CM000679.2:g.7654517G= GRCh38
NC_000017.10:g.7557835G= , CM000679.1:g.7557835G= GRCh37
NC_000017.9:g.7498560G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000250111.9:c.553-111G= MANE Select ENSP00000250111.4:n.553-111G=
ENST00000250111.8:c.553-111G= ENSP00000250111.4:n.553-111G=
ENST00000577026.5:c.307-111G= ENSP00000459145.1:n.307-111G=
ENST00000577113.1:c.150-111G=
NM_001303263.1:c.307-111G= NP_001290192.1:n.307-111G=
NM_001678.4:c.553-111G= NP_001669.3:n.553-111G=
NM_001678.5:c.553-111G= MANE Select NP_001669.3:n.553-111G=
NM_001303263.2:c.307-111G= NP_001290192.1:n.307-111G=
Search 100 bp 5'
Search 100 bp 3'