Canonical Allele Identifier: CA1763924564
Gene: BLK HGNC NCBI

Linked Data

dbSNP Id: rs1798174637

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11491554A>G , CM000670.2:g.11491554A>G GRCh38
NC_000008.10:g.11349063A>G , CM000670.1:g.11349063A>G GRCh37
NC_000008.9:g.11386472A>G NCBI36
NG_023543.1:g.2543A>G
NG_023543.2:g.2543A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696154.2:n.274+4387A>G
ENST00000696154.1:c.-91+4387A>G ENSP00000512445.1:n.-91+4387A>G
ENST00000645242.1:c.-91+4387A>G ENSP00000494690.1:n.-91+4387A>G