Canonical Allele Identifier: CA172067307

Gene: BLK

Linked Data

• dbSNP Id: rs998590479
• MyVariant Identifiers: chr8:g.11349167A>G (hg19) ; chr8:g.11491658A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11491658A>G , CM000670.2:g.11491658A>G	GRCh38
NC_000008.10:g.11349167A>G , CM000670.1:g.11349167A>G	GRCh37
NC_000008.9:g.11386576A>G	NCBI36
NG_023543.1:g.2647A>G
NG_023543.2:g.2647A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.274+4491A>G
ENST00000696154.1:c.-91+4491A>G	ENSP00000512445.1:n.-91+4491A>G
ENST00000645242.1:c.-91+4491A>G	ENSP00000494690.1:n.-91+4491A>G