Canonical Allele Identifier: CA10604204

Gene: DNAJB6

Linked Data

• ClinVar Variation Id: 282521
• ClinVar RCV Id: RCV000379729 ; RCV001500584
• dbSNP Id: rs886042415
• gnomAD v4: 7-157384857-T-G
• MyVariant Identifiers: chr7:g.157177551T>G (hg19) ; chr7:g.157384857T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.157384857T>G , CM000669.2:g.157384857T>G	GRCh38
NC_000007.13:g.157177551T>G , CM000669.1:g.157177551T>G	GRCh37
NC_000007.12:g.156870312T>G	NCBI36
NG_032573.1:g.52842T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262177.9:c.479-10T>G MANE Select	ENSP00000262177.4:n.479-10T>G
ENST00000262177.8:c.479-10T>G	ENSP00000262177.4:n.479-10T>G
ENST00000417758.5:c.479-10T>G	ENSP00000400665.1:n.479-10T>G
ENST00000429029.6:c.479-10T>G	ENSP00000397556.2:n.479-10T>G
ENST00000443280.5:c.346+17374T>G	ENSP00000396267.1:n.346+17374T>G
ENST00000459889.5:c.479-10T>G	ENSP00000488263.1:n.479-10T>G
ENST00000465908.5:n.275-10T>G
ENST00000468928.5:n.784-10T>G
ENST00000487480.1:n.4254-10T>G
ENST00000634080.1:c.479-10T>G	ENSP00000488740.1:n.479-10T>G
NM_005494.2:c.479-10T>G	NP_005485.1:n.479-10T>G
NM_058246.3:c.479-10T>G	NP_490647.1:n.479-10T>G
XM_005249515.2:c.479-10T>G	XP_005249572.1:n.479-10T>G
XM_005249516.2:c.479-10T>G	XP_005249573.1:n.479-10T>G
XM_006715823.1:c.479-10T>G	XP_006715886.1:n.479-10T>G
XM_011515704.1:c.479-10T>G	XP_011514006.1:n.479-10T>G
NM_001363676.1:c.346+17374T>G	NP_001350605.1:n.346+17374T>G
XM_005249515.3:c.479-10T>G	XP_005249572.1:n.479-10T>G
XM_006715823.2:c.479-10T>G	XP_006715886.1:n.479-10T>G
NM_058246.4:c.479-10T>G MANE Select	NP_490647.1:n.479-10T>G
NM_005494.3:c.479-10T>G	NP_005485.1:n.479-10T>G