Canonical Allele Identifier: CA358875

Gene: DNAJB6

Linked Data

• ClinVar Variation Id: 225174
• ClinVar RCV Id: RCV000210839
• dbSNP Id: rs869320700
• MyVariant Identifiers: chr7:g.157160129T>G (hg19) ; chr7:g.157367435T>G (hg38)
• PubMed: PMID:10489050 ; PMID:26205529

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.157367435T>G , CM000669.2:g.157367435T>G	GRCh38
NC_000007.13:g.157160129T>G , CM000669.1:g.157160129T>G	GRCh37
NC_000007.12:g.156852890T>G	NCBI36
NG_032573.1:g.35420T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262177.9:c.298T>G MANE Select	ENSP00000262177.4:p.Phe100Val
ENST00000262177.8:c.298T>G	ENSP00000262177.4:p.Phe100Val
ENST00000412557.5:c.298T>G	ENSP00000403407.1:p.Phe100Val
ENST00000417758.5:c.298T>G	ENSP00000400665.1:p.Phe100Val
ENST00000429029.6:c.298T>G	ENSP00000397556.2:p.Phe100Val
ENST00000441291.5:c.298T>G	ENSP00000415201.1:p.Phe100Val
ENST00000441561.5:c.298T>G	ENSP00000410643.1:p.Phe100Val
ENST00000443280.5:c.298T>G	ENSP00000396267.1:p.Phe100Val
ENST00000459889.5:c.298T>G	ENSP00000488263.1:p.Phe100Val
ENST00000486083.6:n.465T>G
ENST00000488001.5:n.444T>G
ENST00000634080.1:c.298T>G	ENSP00000488740.1:p.Phe100Val
NM_005494.2:c.298T>G	NP_005485.1:p.Phe100Val
NM_058246.3:c.298T>G	NP_490647.1:p.Phe100Val
XM_005249515.2:c.298T>G	XP_005249572.1:p.Phe100Val
XM_005249516.2:c.298T>G	XP_005249573.1:p.Phe100Val
XM_006715823.1:c.298T>G	XP_006715886.1:p.Phe100Val
XM_011515704.1:c.298T>G	XP_011514006.1:p.Phe100Val
NM_001363676.1:c.298T>G	NP_001350605.1:p.Phe100Val
XM_005249515.3:c.298T>G	XP_005249572.1:p.Phe100Val
XM_006715823.2:c.298T>G	XP_006715886.1:p.Phe100Val
NM_058246.4:c.298T>G MANE Select	NP_490647.1:p.Phe100Val
NM_005494.3:c.298T>G	NP_005485.1:p.Phe100Val