Canonical Allele Identifier: CA89106296

Gene: DNAJC19

Linked Data

• dbSNP Id: rs934758233
• gnomAD v3: 3-180984053-A-C
• gnomAD v4: 3-180984053-A-C
• MyVariant Identifiers: chr3:g.180701841A>C (hg19) ; chr3:g.180984053A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180984053A>C , CM000665.2:g.180984053A>C	GRCh38
NC_000003.11:g.180701841A>C , CM000665.1:g.180701841A>C	GRCh37
NC_000003.10:g.182184535A>C	NCBI36
NG_022933.1:g.10722T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000482363.2:n.3051T>G
ENST00000688055.1:c.*1865T>G	ENSP00000508688.1:n.*1865T>G
ENST00000382564.8:c.*587T>G MANE Select	ENSP00000372005.2:n.*587T>G
ENST00000382564.6:c.*587T>G	ENSP00000372005.2:n.*587T>G
ENST00000469657.5:c.*714T>G	ENSP00000418058.1:n.*714T>G
NM_001190233.1:c.*587T>G	NP_001177162.1:n.*587T>G
NM_145261.3:c.*587T>G	NP_660304.1:n.*587T>G
NR_033721.1:n.1058T>G
NR_033722.1:n.1030T>G
NR_033723.1:n.1055T>G
NR_046073.1:n.904T>G
NM_145261.4:c.*587T>G MANE Select	NP_660304.1:n.*587T>G
NM_001190233.2:c.*587T>G	NP_001177162.1:n.*587T>G
NR_033721.2:n.1020T>G
NR_033722.2:n.992T>G