Canonical Allele Identifier: CA845915607
Gene: BLK HGNC NCBI

Linked Data

dbSNP Id: rs1318729848
gnomAD v3: 8-11491682-C-T
gnomAD v4: 8-11491682-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11491682C>T , CM000670.2:g.11491682C>T GRCh38
NC_000008.10:g.11349191C>T , CM000670.1:g.11349191C>T GRCh37
NC_000008.9:g.11386600C>T NCBI36
NG_023543.1:g.2671C>T
NG_023543.2:g.2671C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696154.2:n.274+4515C>T
ENST00000696154.1:c.-91+4515C>T ENSP00000512445.1:n.-91+4515C>T
ENST00000645242.1:c.-91+4515C>T ENSP00000494690.1:n.-91+4515C>T