Canonical Allele Identifier: CA459320837

Gene: BLK

Linked Data

• dbSNP Id: rs1185486598
• gnomAD v2: 8-11421503-C-G
• gnomAD v4: 8-11563994-C-G
• MyVariant Identifiers: chr8:g.11421503C>G (hg19) ; chr8:g.11563994C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11563994C>G , CM000670.2:g.11563994C>G	GRCh38
NC_000008.10:g.11421503C>G , CM000670.1:g.11421503C>G	GRCh37
NC_000008.9:g.11458912C>G	NCBI36
NG_023543.1:g.74983C>G
NG_023543.2:g.74983C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1512C>G
ENST00000696154.1:c.*722C>G	ENSP00000512445.1:n.*722C>G
ENST00000696155.1:n.288C>G
ENST00000259089.9:c.1404C>G MANE Select	ENSP00000259089.4:p.Val468=
ENST00000645242.1:c.1191C>G	ENSP00000494690.1:p.Val397=
ENST00000259089.8:c.1404C>G	ENSP00000259089.4:p.Val468=
ENST00000526097.1:n.1344C>G
ENST00000529894.1:c.1191C>G	ENSP00000433663.1:p.Val397=
NM_001715.2:c.1404C>G	NP_001706.2:p.Val468=
XM_011543824.1:c.1482C>G	XP_011542126.1:p.Val494=
XM_011543825.1:c.1482C>G	XP_011542127.1:p.Val494=
XM_011543826.1:c.1482C>G	XP_011542128.1:p.Val494=
XM_011543827.1:c.1269C>G	XP_011542129.1:p.Val423=
NM_001330465.1:c.1191C>G	NP_001317394.1:p.Val397=
XM_011543825.3:c.1482C>G	XP_011542127.1:p.Val494=
NM_001715.3:c.1404C>G MANE Select	NP_001706.2:p.Val468=
NM_001330465.2:c.1191C>G	NP_001317394.1:p.Val397=