Canonical Allele Identifier: CA367826673
Gene: DNAJC30 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.73097348C>A (hg19) chr7:g.73683018C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73683018C>A , CM000669.2:g.73683018C>A GRCh38
NC_000007.13:g.73097348C>A , CM000669.1:g.73097348C>A GRCh37
NC_000007.12:g.72735284C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395176.3:c.406G>T MANE Select ENSP00000378605.1:p.Gly136Cys
ENST00000395176.2:c.406G>T ENSP00000378605.1:p.Gly136Cys
NM_032317.2:c.406G>T NP_115693.2:p.Gly136Cys
NM_032317.3:c.406G>T MANE Select NP_115693.2:p.Gly136Cys
Search 100 bp 5'
Search 100 bp 3'