Canonical Allele Identifier: CA579798848

Gene: BLK

Linked Data

• dbSNP Id: rs1326745419
• gnomAD v2: 8-11421621-G-C
• MyVariant Identifiers: chr8:g.11421621G>C (hg19) ; chr8:g.11564112G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11564112G>C , CM000670.2:g.11564112G>C	GRCh38
NC_000008.10:g.11421621G>C , CM000670.1:g.11421621G>C	GRCh37
NC_000008.9:g.11459030G>C	NCBI36
NG_023543.1:g.75101G>C
NG_023543.2:g.75101G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1630G>C
ENST00000696154.1:c.*840G>C	ENSP00000512445.1:n.*840G>C
ENST00000696155.1:n.406G>C
ENST00000259089.9:c.*4G>C MANE Select	ENSP00000259089.4:n.*4G>C
ENST00000645242.1:c.*4G>C	ENSP00000494690.1:n.*4G>C
ENST00000259089.8:c.*4G>C	ENSP00000259089.4:n.*4G>C
ENST00000526097.1:n.1462G>C
ENST00000529894.1:c.*4G>C	ENSP00000433663.1:n.*4G>C
NM_001715.2:c.*4G>C	NP_001706.2:n.*4G>C
XM_011543824.1:c.*4G>C	XP_011542126.1:n.*4G>C
XM_011543825.1:c.*4G>C	XP_011542127.1:n.*4G>C
XM_011543826.1:c.*4G>C	XP_011542128.1:n.*4G>C
XM_011543827.1:c.*4G>C	XP_011542129.1:n.*4G>C
NM_001330465.1:c.*4G>C	NP_001317394.1:n.*4G>C
XM_011543825.3:c.*4G>C	XP_011542127.1:n.*4G>C
NM_001715.3:c.*4G>C MANE Select	NP_001706.2:n.*4G>C
NM_001330465.2:c.*4G>C	NP_001317394.1:n.*4G>C