Canonical Allele Identifier: CA1110720712
Gene: BLK HGNC NCBI

Linked Data

dbSNP Id: rs1798176557

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11491700_11491713del , CM000670.2:g.11491700_11491713del GRCh38
NC_000008.10:g.11349209_11349222del , CM000670.1:g.11349209_11349222del GRCh37
NC_000008.9:g.11386618_11386631del NCBI36
NG_023543.1:g.2689_2702del
NG_023543.2:g.2689_2702del

Transcript Alleles

HGVS Amino-acid change
ENST00000696154.2:n.274+4533_274+4546del
ENST00000696154.1:c.-91+4533_-91+4546del ENSP00000512445.1:n.-91+4533_-91+4546del
ENST00000645242.1:c.-91+4533_-91+4546del ENSP00000494690.1:n.-91+4533_-91+4546del