Canonical Allele Identifier: CA710261898
Gene: BDKRB2 HGNC NCBI

Linked Data

dbSNP Id: rs1452949810

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.96205031_96205039del , CM000676.2:g.96205031_96205039del GRCh38
NC_000014.8:g.96671368_96671376del , CM000676.1:g.96671368_96671376del GRCh37
NC_000014.7:g.95741121_95741129del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000554311.2:c.-40+72_-40+80del MANE Select ENSP00000450482.1:n.-40+72_-40+80del
ENST00000539359.1:c.-282+72_-282+80del ENSP00000438376.1:n.-282+72_-282+80del
ENST00000542454.2:c.-2808+72_-2808+80del ENSP00000439459.2:n.-2808+72_-2808+80del
ENST00000553811.1:c.-35+72_-35+80del ENSP00000450984.1:n.-35+72_-35+80del
ENST00000554311.1:c.-40+72_-40+80del ENSP00000450482.1:n.-40+72_-40+80del
NM_000623.3:c.-35+72_-35+80del NP_000614.1:n.-35+72_-35+80del
NM_000623.4:c.-35+72_-35+80del NP_000614.1:n.-35+72_-35+80del
NM_001379692.1:c.-40+72_-40+80del MANE Select NP_001366621.1:n.-40+72_-40+80del