Canonical Allele Identifier: CA2716491433
Gene: BLK HGNC NCBI

Linked Data

dbSNP Id: rs2117206477

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11491504C>T , CM000670.2:g.11491504C>T GRCh38
NC_000008.10:g.11349013C>T , CM000670.1:g.11349013C>T GRCh37
NC_000008.9:g.11386422C>T NCBI36
NG_023543.1:g.2493C>T
NG_023543.2:g.2493C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000696154.2:n.274+4337C>T
ENST00000696154.1:c.-91+4337C>T ENSP00000512445.1:n.-91+4337C>T
ENST00000645242.1:c.-91+4337C>T ENSP00000494690.1:n.-91+4337C>T