Canonical Allele Identifier: CA367826665

Gene: DNAJC30

Linked Data

• MyVariant Identifiers: chr7:g.73097347C>G (hg19) ; chr7:g.73683017C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73683017C>G , CM000669.2:g.73683017C>G	GRCh38
NC_000007.13:g.73097347C>G , CM000669.1:g.73097347C>G	GRCh37
NC_000007.12:g.72735283C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395176.3:c.407G>C MANE Select	ENSP00000378605.1:p.Gly136Ala
ENST00000395176.2:c.407G>C	ENSP00000378605.1:p.Gly136Ala
NM_032317.2:c.407G>C	NP_115693.2:p.Gly136Ala
NM_032317.3:c.407G>C MANE Select	NP_115693.2:p.Gly136Ala