Canonical Allele Identifier: CA1763924572
Gene: BLK HGNC NCBI

Linked Data

dbSNP Id: rs1798174787

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11491567T>G , CM000670.2:g.11491567T>G GRCh38
NC_000008.10:g.11349076T>G , CM000670.1:g.11349076T>G GRCh37
NC_000008.9:g.11386485T>G NCBI36
NG_023543.1:g.2556T>G
NG_023543.2:g.2556T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000696154.2:n.274+4400T>G
ENST00000696154.1:c.-91+4400T>G ENSP00000512445.1:n.-91+4400T>G
ENST00000645242.1:c.-91+4400T>G ENSP00000494690.1:n.-91+4400T>G