Canonical Allele Identifier: CA1763924629
Gene: BLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11491678T= , CM000670.2:g.11491678T= GRCh38
NC_000008.10:g.11349187T= , CM000670.1:g.11349187T= GRCh37
NC_000008.9:g.11386596T= NCBI36
NG_023543.1:g.2667T=
NG_023543.2:g.2667T=

Transcript Alleles

HGVS Amino-acid change
ENST00000696154.2:n.274+4511T=
ENST00000696154.1:c.-91+4511T= ENSP00000512445.1:n.-91+4511T=
ENST00000645242.1:c.-91+4511T= ENSP00000494690.1:n.-91+4511T=