Canonical Allele Identifier: CA367826438
Gene: DNAJC30 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.73097308T>G (hg19) chr7:g.73682978T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73682978T>G , CM000669.2:g.73682978T>G GRCh38
NC_000007.13:g.73097308T>G , CM000669.1:g.73097308T>G GRCh37
NC_000007.12:g.72735244T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395176.3:c.446A>C MANE Select ENSP00000378605.1:p.Asp149Ala
ENST00000395176.2:c.446A>C ENSP00000378605.1:p.Asp149Ala
NM_032317.2:c.446A>C NP_115693.2:p.Asp149Ala
NM_032317.3:c.446A>C MANE Select NP_115693.2:p.Asp149Ala
Search 100 bp 5'
Search 100 bp 3'