Canonical Allele Identifier: CA1763964578
Gene: BLK HGNC NCBI

Linked Data

dbSNP Id: rs1801648765
gnomAD v4: 8-11564600-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11564600G>T , CM000670.2:g.11564600G>T GRCh38
NC_000008.10:g.11422109G>T , CM000670.1:g.11422109G>T GRCh37
NC_000008.9:g.11459518G>T NCBI36
NG_023543.1:g.75589G>T
NG_023543.2:g.75589G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000259089.8:c.*492G>T ENSP00000259089.4:n.*492G>T
NM_001330465.1:c.*492G>T NP_001317394.1:n.*492G>T