Canonical Allele Identifier: CA845915395
Gene: BLK HGNC NCBI

Linked Data

dbSNP Id: rs1208569087

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11491323C>T , CM000670.2:g.11491323C>T GRCh38
NC_000008.10:g.11348832C>T , CM000670.1:g.11348832C>T GRCh37
NC_000008.9:g.11386241C>T NCBI36
NG_023543.1:g.2312C>T
NG_023543.2:g.2312C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000696154.2:n.274+4156C>T
ENST00000696154.1:c.-91+4156C>T ENSP00000512445.1:n.-91+4156C>T
ENST00000645242.1:c.-91+4156C>T ENSP00000494690.1:n.-91+4156C>T