Canonical Allele Identifier: CA2538845636
Gene: BLK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11491632T>C , CM000670.2:g.11491632T>C GRCh38
NC_000008.10:g.11349141T>C , CM000670.1:g.11349141T>C GRCh37
NC_000008.9:g.11386550T>C NCBI36
NG_023543.1:g.2621T>C
NG_023543.2:g.2621T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000696154.2:n.274+4465T>C
ENST00000696154.1:c.-91+4465T>C ENSP00000512445.1:n.-91+4465T>C
ENST00000645242.1:c.-91+4465T>C ENSP00000494690.1:n.-91+4465T>C