Canonical Allele Identifier: CA2537072997
Gene: BLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11491378A>G , CM000670.2:g.11491378A>G GRCh38
NC_000008.10:g.11348887A>G , CM000670.1:g.11348887A>G GRCh37
NC_000008.9:g.11386296A>G NCBI36
NG_023543.1:g.2367A>G
NG_023543.2:g.2367A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696154.2:n.274+4211A>G
ENST00000696154.1:c.-91+4211A>G ENSP00000512445.1:n.-91+4211A>G
ENST00000645242.1:c.-91+4211A>G ENSP00000494690.1:n.-91+4211A>G