Canonical Allele Identifier: CA2559515688
Gene: BLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11491681G>A , CM000670.2:g.11491681G>A GRCh38
NC_000008.10:g.11349190G>A , CM000670.1:g.11349190G>A GRCh37
NC_000008.9:g.11386599G>A NCBI36
NG_023543.1:g.2670G>A
NG_023543.2:g.2670G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696154.2:n.274+4514G>A
ENST00000696154.1:c.-91+4514G>A ENSP00000512445.1:n.-91+4514G>A
ENST00000645242.1:c.-91+4514G>A ENSP00000494690.1:n.-91+4514G>A