Canonical Allele Identifier: CA4289924
Gene: DNAJC30 HGNC NCBI

Linked Data

dbSNP Id: rs782347951
gnomAD v2: 7-73097341-G-C
gnomAD v3: 7-73683011-G-C
gnomAD v4: 7-73683011-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73683011G>C , CM000669.2:g.73683011G>C GRCh38
NC_000007.13:g.73097341G>C , CM000669.1:g.73097341G>C GRCh37
NC_000007.12:g.72735277G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395176.3:c.413C>G MANE Select ENSP00000378605.1:p.Pro138Arg
ENST00000395176.2:c.413C>G ENSP00000378605.1:p.Pro138Arg
NM_032317.2:c.413C>G NP_115693.2:p.Pro138Arg
NM_032317.3:c.413C>G MANE Select NP_115693.2:p.Pro138Arg