Canonical Allele Identifier: CA172067042

Gene: BLK

Linked Data

• dbSNP Id: rs192450053
• MyVariant Identifiers: chr8:g.11348934A>T (hg19) ; chr8:g.11491425A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11491425A>T , CM000670.2:g.11491425A>T	GRCh38
NC_000008.10:g.11348934A>T , CM000670.1:g.11348934A>T	GRCh37
NC_000008.9:g.11386343A>T	NCBI36
NG_023543.1:g.2414A>T
NG_023543.2:g.2414A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.274+4258A>T
ENST00000696154.1:c.-91+4258A>T	ENSP00000512445.1:n.-91+4258A>T
ENST00000645242.1:c.-91+4258A>T	ENSP00000494690.1:n.-91+4258A>T