Canonical Allele Identifier: CA367826441
Gene: DNAJC30 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.73097309C>A (hg19) chr7:g.73682979C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73682979C>A , CM000669.2:g.73682979C>A GRCh38
NC_000007.13:g.73097309C>A , CM000669.1:g.73097309C>A GRCh37
NC_000007.12:g.72735245C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395176.3:c.445G>T MANE Select ENSP00000378605.1:p.Asp149Tyr
ENST00000395176.2:c.445G>T ENSP00000378605.1:p.Asp149Tyr
NM_032317.2:c.445G>T NP_115693.2:p.Asp149Tyr
NM_032317.3:c.445G>T MANE Select NP_115693.2:p.Asp149Tyr
Search 100 bp 5'
Search 100 bp 3'