Canonical Allele Identifier: CA172067010
Gene: BLK HGNC NCBI

Linked Data

dbSNP Id: rs1554536649

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11491410del , CM000670.2:g.11491410del GRCh38
NC_000008.10:g.11348919del , CM000670.1:g.11348919del GRCh37
NC_000008.9:g.11386328del NCBI36
NG_023543.1:g.2399del
NG_023543.2:g.2399del

Transcript Alleles

HGVS Amino-acid Change
ENST00000696154.2:n.274+4243del
ENST00000696154.1:c.-91+4243del ENSP00000512445.1:n.-91+4243del
ENST00000645242.1:c.-91+4243del ENSP00000494690.1:n.-91+4243del