Canonical Allele Identifier: CA367826476
Gene: DNAJC30 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.73097312G>C (hg19) chr7:g.73682982G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73682982G>C , CM000669.2:g.73682982G>C GRCh38
NC_000007.13:g.73097312G>C , CM000669.1:g.73097312G>C GRCh37
NC_000007.12:g.72735248G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395176.3:c.442C>G MANE Select ENSP00000378605.1:p.His148Asp
ENST00000395176.2:c.442C>G ENSP00000378605.1:p.His148Asp
NM_032317.2:c.442C>G NP_115693.2:p.His148Asp
NM_032317.3:c.442C>G MANE Select NP_115693.2:p.His148Asp
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