Canonical Allele Identifier: CA259941
Gene: DNAJB6 HGNC NCBI

Linked Data

ClinVar Variation Id: 30905
ClinVar RCV Id: RCV000023892 RCV000594360
dbSNP Id: rs387907047
MyVariant Identifiers: chr7:g.157160118C>G (hg19) chr7:g.157367424C>G (hg38)
PubMed: PMID:22334415 PMID:23891399
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.157367424C>G , CM000669.2:g.157367424C>G GRCh38
NC_000007.13:g.157160118C>G , CM000669.1:g.157160118C>G GRCh37
NC_000007.12:g.156852879C>G NCBI36
NG_032573.1:g.35409C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262177.9:c.287C>G MANE Select ENSP00000262177.4:p.Pro96Arg
ENST00000262177.8:c.287C>G ENSP00000262177.4:p.Pro96Arg
ENST00000412557.5:c.287C>G ENSP00000403407.1:p.Pro96Arg
ENST00000417758.5:c.287C>G ENSP00000400665.1:p.Pro96Arg
ENST00000429029.6:c.287C>G ENSP00000397556.2:p.Pro96Arg
ENST00000441291.5:c.287C>G ENSP00000415201.1:p.Pro96Arg
ENST00000441561.5:c.287C>G ENSP00000410643.1:p.Pro96Arg
ENST00000443280.5:c.287C>G ENSP00000396267.1:p.Pro96Arg
ENST00000453383.5:c.287C>G ENSP00000396240.1:p.Pro96Arg
ENST00000459889.5:c.287C>G ENSP00000488263.1:p.Pro96Arg
ENST00000486083.6:n.454C>G
ENST00000488001.5:n.433C>G
ENST00000634080.1:c.287C>G ENSP00000488740.1:p.Pro96Arg
NM_005494.2:c.287C>G NP_005485.1:p.Pro96Arg
NM_058246.3:c.287C>G NP_490647.1:p.Pro96Arg
XM_005249515.2:c.287C>G XP_005249572.1:p.Pro96Arg
XM_005249516.2:c.287C>G XP_005249573.1:p.Pro96Arg
XM_006715823.1:c.287C>G XP_006715886.1:p.Pro96Arg
XM_011515704.1:c.287C>G XP_011514006.1:p.Pro96Arg
NM_001363676.1:c.287C>G NP_001350605.1:p.Pro96Arg
XM_005249515.3:c.287C>G XP_005249572.1:p.Pro96Arg
XM_006715823.2:c.287C>G XP_006715886.1:p.Pro96Arg
NM_058246.4:c.287C>G MANE Select NP_490647.1:p.Pro96Arg
NM_005494.3:c.287C>G NP_005485.1:p.Pro96Arg
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Search 100 bp 3'