Canonical Allele Identifier: CA2686158943
Gene: BLK HGNC NCBI

Linked Data

gnomAD v4: 8-11564601-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11564601C>T , CM000670.2:g.11564601C>T GRCh38
NC_000008.10:g.11422110C>T , CM000670.1:g.11422110C>T GRCh37
NC_000008.9:g.11459519C>T NCBI36
NG_023543.1:g.75590C>T
NG_023543.2:g.75590C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000259089.8:c.*493C>T ENSP00000259089.4:n.*493C>T
NM_001330465.1:c.*493C>T NP_001317394.1:n.*493C>T
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