Canonical Allele Identifier: CA845991690

Gene: BLK

Linked Data

• dbSNP Id: rs1304016690
• gnomAD v3: 8-11564567-G-A
• gnomAD v4: 8-11564567-G-A
• MyVariant Identifiers: chr8:g.11422076G>A (hg19) ; chr8:g.11564567G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564567G>A , CM000670.2:g.11564567G>A	GRCh38
NC_000008.10:g.11422076G>A , CM000670.1:g.11422076G>A	GRCh37
NC_000008.9:g.11459485G>A	NCBI36
NG_023543.1:g.75556G>A
NG_023543.2:g.75556G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.2085G>A
ENST00000696154.1:c.*1295G>A	ENSP00000512445.1:n.*1295G>A
ENST00000259089.9:c.*459G>A MANE Select	ENSP00000259089.4:n.*459G>A
ENST00000645242.1:c.*459G>A	ENSP00000494690.1:n.*459G>A
ENST00000259089.8:c.*459G>A	ENSP00000259089.4:n.*459G>A
ENST00000526097.1:n.1917G>A
NM_001715.2:c.*459G>A	NP_001706.2:n.*459G>A
XM_011543824.1:c.*459G>A	XP_011542126.1:n.*459G>A
XM_011543825.1:c.*459G>A	XP_011542127.1:n.*459G>A
XM_011543826.1:c.*459G>A	XP_011542128.1:n.*459G>A
XM_011543827.1:c.*459G>A	XP_011542129.1:n.*459G>A
NM_001330465.1:c.*459G>A	NP_001317394.1:n.*459G>A
XM_011543825.3:c.*459G>A	XP_011542127.1:n.*459G>A
NM_001715.3:c.*459G>A MANE Select	NP_001706.2:n.*459G>A
NM_001330465.2:c.*459G>A	NP_001317394.1:n.*459G>A