Canonical Allele Identifier: CA966266180
Gene: BDKRB2 HGNC NCBI

Linked Data

dbSNP Id: rs1890140151
gnomAD v3: 14-96205000-G-A
gnomAD v4: 14-96205000-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.96205000G>A , CM000676.2:g.96205000G>A GRCh38
NC_000014.8:g.96671337G>A , CM000676.1:g.96671337G>A GRCh37
NC_000014.7:g.95741090G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000554311.2:c.-40+41G>A MANE Select ENSP00000450482.1:n.-40+41G>A
ENST00000539359.1:c.-282+41G>A ENSP00000438376.1:n.-282+41G>A
ENST00000542454.2:c.-2808+41G>A ENSP00000439459.2:n.-2808+41G>A
ENST00000553811.1:c.-35+41G>A ENSP00000450984.1:n.-35+41G>A
ENST00000554311.1:c.-40+41G>A ENSP00000450482.1:n.-40+41G>A
NM_000623.3:c.-35+41G>A NP_000614.1:n.-35+41G>A
NM_000623.4:c.-35+41G>A NP_000614.1:n.-35+41G>A
NM_001379692.1:c.-40+41G>A MANE Select NP_001366621.1:n.-40+41G>A
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