Canonical Allele Identifier: CA266012948
Gene: BDKRB2 HGNC NCBI

Linked Data

dbSNP Id: rs776719790
MyVariant Identifiers: chr14:g.96671220_96671227del (hg19) chr14:g.96204883_96204890del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.96204883_96204890del , CM000676.2:g.96204883_96204890del GRCh38
NC_000014.8:g.96671220_96671227del , CM000676.1:g.96671220_96671227del GRCh37
NC_000014.7:g.95740973_95740980del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000554311.2:c.-116_-109del MANE Select ENSP00000450482.1:n.-116_-109del
ENST00000539359.1:c.-358_-351del ENSP00000438376.1:n.-358_-351del
ENST00000542454.2:c.-2884_-2877del ENSP00000439459.2:n.-2884_-2877del
ENST00000553811.1:c.-111_-104del ENSP00000450984.1:n.-111_-104del
ENST00000554311.1:c.-116_-109del ENSP00000450482.1:n.-116_-109del
NM_000623.3:c.-111_-104del NP_000614.1:n.-111_-104del
NM_000623.4:c.-111_-104del NP_000614.1:n.-111_-104del
NM_001379692.1:c.-116_-109del MANE Select NP_001366621.1:n.-116_-109del
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