Canonical Allele Identifier: CA2686158940
Gene: BLK HGNC NCBI

Linked Data

gnomAD v4: 8-11564600-G-A
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Genomic Alleles

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

Transcript Alleles

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