Canonical Allele Identifier: CA1763924471
Gene: BLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11491396G= , CM000670.2:g.11491396G= GRCh38
NC_000008.10:g.11348905G= , CM000670.1:g.11348905G= GRCh37
NC_000008.9:g.11386314G= NCBI36
NG_023543.1:g.2385G=
NG_023543.2:g.2385G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696154.2:n.274+4229G=
ENST00000696154.1:c.-91+4229G= ENSP00000512445.1:n.-91+4229G=
ENST00000645242.1:c.-91+4229G= ENSP00000494690.1:n.-91+4229G=