Canonical Allele Identifier: CA459320728

Gene: BLK

Linked Data

• dbSNP Id: rs1356289485
• gnomAD v3: 8-11563961-C-G
• gnomAD v4: 8-11563961-C-G
• MyVariant Identifiers: chr8:g.11421470C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11563961C>G , CM000670.2:g.11563961C>G	GRCh38
NC_000008.10:g.11421470C>G , CM000670.1:g.11421470C>G	GRCh37
NC_000008.9:g.11458879C>G	NCBI36
NG_023543.1:g.74950C>G
NG_023543.2:g.74950C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696154.2:n.1479C>G
ENST00000696154.1:c.*689C>G	ENSP00000512445.1:n.*689C>G
ENST00000696155.1:n.255C>G
ENST00000259089.9:c.1371C>G MANE Select	ENSP00000259089.4:p.Pro457=
ENST00000645242.1:c.1158C>G	ENSP00000494690.1:p.Pro386=
ENST00000259089.8:c.1371C>G	ENSP00000259089.4:p.Pro457=
ENST00000526097.1:n.1311C>G
ENST00000529894.1:c.1158C>G	ENSP00000433663.1:p.Pro386=
NM_001715.2:c.1371C>G	NP_001706.2:p.Pro457=
XM_011543824.1:c.1449C>G	XP_011542126.1:p.Pro483=
XM_011543825.1:c.1449C>G	XP_011542127.1:p.Pro483=
XM_011543826.1:c.1449C>G	XP_011542128.1:p.Pro483=
XM_011543827.1:c.1236C>G	XP_011542129.1:p.Pro412=
NM_001330465.1:c.1158C>G	NP_001317394.1:p.Pro386=
XM_011543825.3:c.1449C>G	XP_011542127.1:p.Pro483=
NM_001715.3:c.1371C>G MANE Select	NP_001706.2:p.Pro457=
NM_001330465.2:c.1158C>G	NP_001317394.1:p.Pro386=