Canonical Allele Identifier: CA172067009
Gene: BLK HGNC NCBI

Linked Data

dbSNP Id: rs879188145
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11491409_11491410delinsA , CM000670.2:g.11491409_11491410delinsA GRCh38
NC_000008.10:g.11348918_11348919delinsA , CM000670.1:g.11348918_11348919delinsA GRCh37
NC_000008.9:g.11386327_11386328delinsA NCBI36
NG_023543.1:g.2398_2399delinsA
NG_023543.2:g.2398_2399delinsA

Transcript Alleles

HGVS Amino-acid Change
ENST00000696154.2:n.274+4242_274+4243delinsA
ENST00000696154.1:c.-91+4242_-91+4243delinsA ENSP00000512445.1:n.-91+4242_-91+4243delinsA
ENST00000645242.1:c.-91+4242_-91+4243delinsA ENSP00000494690.1:n.-91+4242_-91+4243delinsA
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