Canonical Allele Identifier: CA4289911
Gene: DNAJC30 HGNC NCBI

Linked Data

dbSNP Id: rs781809516
gnomAD v2: 7-73097299-C-G
gnomAD v4: 7-73682969-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73682969C>G , CM000669.2:g.73682969C>G GRCh38
NC_000007.13:g.73097299C>G , CM000669.1:g.73097299C>G GRCh37
NC_000007.12:g.72735235C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395176.3:c.455G>C MANE Select ENSP00000378605.1:p.Arg152Pro
ENST00000395176.2:c.455G>C ENSP00000378605.1:p.Arg152Pro
NM_032317.2:c.455G>C NP_115693.2:p.Arg152Pro
NM_032317.3:c.455G>C MANE Select NP_115693.2:p.Arg152Pro