Canonical Allele Identifier: CA370316942

Gene: BLK

Linked Data

• dbSNP Id: rs1801613735
• gnomAD v3: 8-11564037-T-G
• gnomAD v4: 8-11564037-T-G
• MyVariant Identifiers: chr8:g.11421546T>G (hg19) ; chr8:g.11564037T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564037T>G , CM000670.2:g.11564037T>G	GRCh38
NC_000008.10:g.11421546T>G , CM000670.1:g.11421546T>G	GRCh37
NC_000008.9:g.11458955T>G	NCBI36
NG_023543.1:g.75026T>G
NG_023543.2:g.75026T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1555T>G
ENST00000696154.1:c.*765T>G	ENSP00000512445.1:n.*765T>G
ENST00000696155.1:n.331T>G
ENST00000259089.9:c.1447T>G MANE Select	ENSP00000259089.4:p.Phe483Val
ENST00000645242.1:c.1234T>G	ENSP00000494690.1:p.Phe412Val
ENST00000259089.8:c.1447T>G	ENSP00000259089.4:p.Phe483Val
ENST00000526097.1:n.1387T>G
ENST00000529894.1:c.1234T>G	ENSP00000433663.1:p.Phe412Val
NM_001715.2:c.1447T>G	NP_001706.2:p.Phe483Val
XM_011543824.1:c.1525T>G	XP_011542126.1:p.Phe509Val
XM_011543825.1:c.1525T>G	XP_011542127.1:p.Phe509Val
XM_011543826.1:c.1525T>G	XP_011542128.1:p.Phe509Val
XM_011543827.1:c.1312T>G	XP_011542129.1:p.Phe438Val
NM_001330465.1:c.1234T>G	NP_001317394.1:p.Phe412Val
XM_011543825.3:c.1525T>G	XP_011542127.1:p.Phe509Val
NM_001715.3:c.1447T>G MANE Select	NP_001706.2:p.Phe483Val
NM_001330465.2:c.1234T>G	NP_001317394.1:p.Phe412Val