Canonical Allele Identifier: CA1763924482
Gene: BLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11491410T= , CM000670.2:g.11491410T= GRCh38
NC_000008.10:g.11348919T= , CM000670.1:g.11348919T= GRCh37
NC_000008.9:g.11386328T= NCBI36
NG_023543.1:g.2399T=
NG_023543.2:g.2399T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696154.2:n.274+4243T=
ENST00000696154.1:c.-91+4243T= ENSP00000512445.1:n.-91+4243T=
ENST00000645242.1:c.-91+4243T= ENSP00000494690.1:n.-91+4243T=