Canonical Allele Identifier: CA370316877

Gene: BLK

Linked Data

• dbSNP Id: rs1215314462
• gnomAD v2: 8-11421526-G-A
• gnomAD v4: 8-11564017-G-A
• MyVariant Identifiers: chr8:g.11421526G>A (hg19) ; chr8:g.11564017G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564017G>A , CM000670.2:g.11564017G>A	GRCh38
NC_000008.10:g.11421526G>A , CM000670.1:g.11421526G>A	GRCh37
NC_000008.9:g.11458935G>A	NCBI36
NG_023543.1:g.75006G>A
NG_023543.2:g.75006G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1535G>A
ENST00000696154.1:c.*745G>A	ENSP00000512445.1:n.*745G>A
ENST00000696155.1:n.311G>A
ENST00000259089.9:c.1427G>A MANE Select	ENSP00000259089.4:p.Arg476Gln
ENST00000645242.1:c.1214G>A	ENSP00000494690.1:p.Arg405Gln
ENST00000259089.8:c.1427G>A	ENSP00000259089.4:p.Arg476Gln
ENST00000526097.1:n.1367G>A
ENST00000529894.1:c.1214G>A	ENSP00000433663.1:p.Arg405Gln
NM_001715.2:c.1427G>A	NP_001706.2:p.Arg476Gln
XM_011543824.1:c.1505G>A	XP_011542126.1:p.Arg502Gln
XM_011543825.1:c.1505G>A	XP_011542127.1:p.Arg502Gln
XM_011543826.1:c.1505G>A	XP_011542128.1:p.Arg502Gln
XM_011543827.1:c.1292G>A	XP_011542129.1:p.Arg431Gln
NM_001330465.1:c.1214G>A	NP_001317394.1:p.Arg405Gln
XM_011543825.3:c.1505G>A	XP_011542127.1:p.Arg502Gln
NM_001715.3:c.1427G>A MANE Select	NP_001706.2:p.Arg476Gln
NM_001330465.2:c.1214G>A	NP_001317394.1:p.Arg405Gln