Canonical Allele Identifier: CA459320849

Gene: BLK

Linked Data

• dbSNP Id: rs1297897319
• gnomAD v2: 8-11421527-G-T
• gnomAD v4: 8-11564018-G-T
• MyVariant Identifiers: chr8:g.11421527G>T (hg19) ; chr8:g.11564018G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564018G>T , CM000670.2:g.11564018G>T	GRCh38
NC_000008.10:g.11421527G>T , CM000670.1:g.11421527G>T	GRCh37
NC_000008.9:g.11458936G>T	NCBI36
NG_023543.1:g.75007G>T
NG_023543.2:g.75007G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1536G>T
ENST00000696154.1:c.*746G>T	ENSP00000512445.1:n.*746G>T
ENST00000696155.1:n.312G>T
ENST00000259089.9:c.1428G>T MANE Select	ENSP00000259089.4:p.Arg476=
ENST00000645242.1:c.1215G>T	ENSP00000494690.1:p.Arg405=
ENST00000259089.8:c.1428G>T	ENSP00000259089.4:p.Arg476=
ENST00000526097.1:n.1368G>T
ENST00000529894.1:c.1215G>T	ENSP00000433663.1:p.Arg405=
NM_001715.2:c.1428G>T	NP_001706.2:p.Arg476=
XM_011543824.1:c.1506G>T	XP_011542126.1:p.Arg502=
XM_011543825.1:c.1506G>T	XP_011542127.1:p.Arg502=
XM_011543826.1:c.1506G>T	XP_011542128.1:p.Arg502=
XM_011543827.1:c.1293G>T	XP_011542129.1:p.Arg431=
NM_001330465.1:c.1215G>T	NP_001317394.1:p.Arg405=
XM_011543825.3:c.1506G>T	XP_011542127.1:p.Arg502=
NM_001715.3:c.1428G>T MANE Select	NP_001706.2:p.Arg476=
NM_001330465.2:c.1215G>T	NP_001317394.1:p.Arg405=