Canonical Allele Identifier: CA710261813
Gene: BDKRB2 HGNC NCBI

Linked Data

dbSNP Id: rs1222702396
MyVariant Identifiers: chr14:g.96671276_96671277insT (hg19) chr14:g.96204939_96204940insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.96204940dup , CM000676.2:g.96204940dup GRCh38
NC_000014.8:g.96671277dup , CM000676.1:g.96671277dup GRCh37
NC_000014.7:g.95741030dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000554311.2:c.-59dup MANE Select ENSP00000450482.1:n.-59dup
ENST00000539359.1:c.-301dup ENSP00000438376.1:n.-301dup
ENST00000542454.2:c.-2827dup ENSP00000439459.2:n.-2827dup
ENST00000553811.1:c.-54dup ENSP00000450984.1:n.-54dup
ENST00000554311.1:c.-59dup ENSP00000450482.1:n.-59dup
NM_000623.3:c.-54dup NP_000614.1:n.-54dup
NM_000623.4:c.-54dup NP_000614.1:n.-54dup
NM_001379692.1:c.-59dup MANE Select NP_001366621.1:n.-59dup
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