Canonical Allele Identifier: CA367826669
Gene: DNAJC30 HGNC NCBI

Linked Data

gnomAD v4: 7-73683018-C-T
MyVariant Identifiers: chr7:g.73097348C>T (hg19) chr7:g.73683018C>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000395176.3:c.406G>A MANE Select ENSP00000378605.1:p.Gly136Ser
ENST00000395176.2:c.406G>A ENSP00000378605.1:p.Gly136Ser
NM_032317.2:c.406G>A NP_115693.2:p.Gly136Ser
NM_032317.3:c.406G>A MANE Select NP_115693.2:p.Gly136Ser
Search 100 bp 5'
Search 100 bp 3'