Canonical Allele Identifier: CA579799586

Gene: BLK

Linked Data

• dbSNP Id: rs1408413860
• gnomAD v2: 8-11422052-C-T
• gnomAD v4: 8-11564543-C-T
• MyVariant Identifiers: chr8:g.11422052C>T (hg19) ; chr8:g.11564543C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564543C>T , CM000670.2:g.11564543C>T	GRCh38
NC_000008.10:g.11422052C>T , CM000670.1:g.11422052C>T	GRCh37
NC_000008.9:g.11459461C>T	NCBI36
NG_023543.1:g.75532C>T
NG_023543.2:g.75532C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.2061C>T
ENST00000696154.1:c.*1271C>T	ENSP00000512445.1:n.*1271C>T
ENST00000259089.9:c.*435C>T MANE Select	ENSP00000259089.4:n.*435C>T
ENST00000645242.1:c.*435C>T	ENSP00000494690.1:n.*435C>T
ENST00000259089.8:c.*435C>T	ENSP00000259089.4:n.*435C>T
ENST00000526097.1:n.1893C>T
NM_001715.2:c.*435C>T	NP_001706.2:n.*435C>T
XM_011543824.1:c.*435C>T	XP_011542126.1:n.*435C>T
XM_011543825.1:c.*435C>T	XP_011542127.1:n.*435C>T
XM_011543826.1:c.*435C>T	XP_011542128.1:n.*435C>T
XM_011543827.1:c.*435C>T	XP_011542129.1:n.*435C>T
NM_001330465.1:c.*435C>T	NP_001317394.1:n.*435C>T
XM_011543825.3:c.*435C>T	XP_011542127.1:n.*435C>T
NM_001715.3:c.*435C>T MANE Select	NP_001706.2:n.*435C>T
NM_001330465.2:c.*435C>T	NP_001317394.1:n.*435C>T