Canonical Allele Identifier: CA1110720736

Gene: BLK

Linked Data

• dbSNP Id: rs1798177014
• gnomAD v3: 8-11491728-G-A
• gnomAD v4: 8-11491728-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11491728G>A , CM000670.2:g.11491728G>A	GRCh38
NC_000008.10:g.11349237G>A , CM000670.1:g.11349237G>A	GRCh37
NC_000008.9:g.11386646G>A	NCBI36
NG_023543.1:g.2717G>A
NG_023543.2:g.2717G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696154.2:n.274+4561G>A
ENST00000696154.1:c.-91+4561G>A	ENSP00000512445.1:n.-91+4561G>A
ENST00000645242.1:c.-91+4561G>A	ENSP00000494690.1:n.-91+4561G>A