Canonical Allele Identifier: CA4290032
Gene: DNAJC30 HGNC NCBI
BUD23 HGNC NCBI

Linked Data

dbSNP Id: rs782382610
gnomAD v2: 7-73097738-A-C
gnomAD v4: 7-73683408-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73683408A>C , CM000669.2:g.73683408A>C GRCh38
NC_000007.13:g.73097738A>C , CM000669.1:g.73097738A>C GRCh37
NC_000007.12:g.72735674A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395176.3:c.16T>G (DNAJC30) MANE Select ENSP00000378605.1:p.Trp6Gly
ENST00000395176.2:c.16T>G (DNAJC30) ENSP00000378605.1:p.Trp6Gly
ENST00000464615.1:n.359+25A>C (BUD23)
NM_032317.2:c.16T>G (DNAJC30) NP_115693.2:p.Trp6Gly
NM_032317.3:c.16T>G (DNAJC30) MANE Select NP_115693.2:p.Trp6Gly