Canonical Allele Identifier: CA370316857

Gene: BLK

Linked Data

• dbSNP Id: rs1428445234
• gnomAD v4: 8-11564010-C-T
• MyVariant Identifiers: chr8:g.11421519C>T (hg19) ; chr8:g.11564010C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564010C>T , CM000670.2:g.11564010C>T	GRCh38
NC_000008.10:g.11421519C>T , CM000670.1:g.11421519C>T	GRCh37
NC_000008.9:g.11458928C>T	NCBI36
NG_023543.1:g.74999C>T
NG_023543.2:g.74999C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1528C>T
ENST00000696154.1:c.*738C>T	ENSP00000512445.1:n.*738C>T
ENST00000696155.1:n.304C>T
ENST00000259089.9:c.1420C>T MANE Select	ENSP00000259089.4:p.Arg474Cys
ENST00000645242.1:c.1207C>T	ENSP00000494690.1:p.Arg403Cys
ENST00000259089.8:c.1420C>T	ENSP00000259089.4:p.Arg474Cys
ENST00000526097.1:n.1360C>T
ENST00000529894.1:c.1207C>T	ENSP00000433663.1:p.Arg403Cys
NM_001715.2:c.1420C>T	NP_001706.2:p.Arg474Cys
XM_011543824.1:c.1498C>T	XP_011542126.1:p.Arg500Cys
XM_011543825.1:c.1498C>T	XP_011542127.1:p.Arg500Cys
XM_011543826.1:c.1498C>T	XP_011542128.1:p.Arg500Cys
XM_011543827.1:c.1285C>T	XP_011542129.1:p.Arg429Cys
NM_001330465.1:c.1207C>T	NP_001317394.1:p.Arg403Cys
XM_011543825.3:c.1498C>T	XP_011542127.1:p.Arg500Cys
NM_001715.3:c.1420C>T MANE Select	NP_001706.2:p.Arg474Cys
NM_001330465.2:c.1207C>T	NP_001317394.1:p.Arg403Cys