Canonical Allele Identifier: CA1110720718
Gene: BLK HGNC NCBI

Linked Data

dbSNP Id: rs1798176698
gnomAD v3: 8-11491712-C-G
gnomAD v4: 8-11491712-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11491712C>G , CM000670.2:g.11491712C>G GRCh38
NC_000008.10:g.11349221C>G , CM000670.1:g.11349221C>G GRCh37
NC_000008.9:g.11386630C>G NCBI36
NG_023543.1:g.2701C>G
NG_023543.2:g.2701C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000696154.2:n.274+4545C>G
ENST00000696154.1:c.-91+4545C>G ENSP00000512445.1:n.-91+4545C>G
ENST00000645242.1:c.-91+4545C>G ENSP00000494690.1:n.-91+4545C>G