Canonical Allele Identifier: CA459308557
Gene: BLK HGNC NCBI

Linked Data

dbSNP Id: rs1300520620
gnomAD v2: 8-11405614-G-A
gnomAD v4: 8-11548105-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11548105G>A , CM000670.2:g.11548105G>A GRCh38
NC_000008.10:g.11405614G>A , CM000670.1:g.11405614G>A GRCh37
NC_000008.9:g.11443023G>A NCBI36
NG_023543.1:g.59094G>A
NG_023543.2:g.59094G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696154.2:n.400G>A
ENST00000696154.1:c.36G>A ENSP00000512445.1:p.Glu12=
ENST00000259089.9:c.249G>A MANE Select ENSP00000259089.4:p.Glu83=
ENST00000645242.1:c.36G>A ENSP00000494690.1:p.Glu12=
ENST00000259089.8:c.249G>A ENSP00000259089.4:p.Glu83=
ENST00000529894.1:c.36G>A ENSP00000433663.1:p.Glu12=
ENST00000533828.1:n.447G>A
NM_001715.2:c.249G>A NP_001706.2:p.Glu83=
XM_011543824.1:c.249G>A XP_011542126.1:p.Glu83=
XM_011543825.1:c.249G>A XP_011542127.1:p.Glu83=
XM_011543826.1:c.249G>A XP_011542128.1:p.Glu83=
XM_011543827.1:c.36G>A XP_011542129.1:p.Glu12=
XM_011543828.1:c.249G>A XP_011542130.1:p.Glu83=
XM_011543829.1:c.249G>A XP_011542131.1:p.Glu83=
NM_001330465.1:c.36G>A NP_001317394.1:p.Glu12=
XM_011543825.3:c.249G>A XP_011542127.1:p.Glu83=
XM_011543828.3:c.249G>A XP_011542130.1:p.Glu83=
XM_011543829.3:c.249G>A XP_011542131.1:p.Glu83=
NM_001715.3:c.249G>A MANE Select NP_001706.2:p.Glu83=
NM_001330465.2:c.36G>A NP_001317394.1:p.Glu12=