Canonical Allele Identifier: CA89106297

Gene: DNAJC19

Linked Data

• dbSNP Id: rs1041026360
• MyVariant Identifiers: chr3:g.180701842T>C (hg19) ; chr3:g.180984054T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180984054T>C , CM000665.2:g.180984054T>C	GRCh38
NC_000003.11:g.180701842T>C , CM000665.1:g.180701842T>C	GRCh37
NC_000003.10:g.182184536T>C	NCBI36
NG_022933.1:g.10721A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000482363.2:n.3050A>G
ENST00000688055.1:c.*1864A>G	ENSP00000508688.1:n.*1864A>G
ENST00000382564.8:c.*586A>G MANE Select	ENSP00000372005.2:n.*586A>G
ENST00000382564.6:c.*586A>G	ENSP00000372005.2:n.*586A>G
ENST00000469657.5:c.*713A>G	ENSP00000418058.1:n.*713A>G
NM_001190233.1:c.*586A>G	NP_001177162.1:n.*586A>G
NM_145261.3:c.*586A>G	NP_660304.1:n.*586A>G
NR_033721.1:n.1057A>G
NR_033722.1:n.1029A>G
NR_033723.1:n.1054A>G
NR_046073.1:n.903A>G
NM_145261.4:c.*586A>G MANE Select	NP_660304.1:n.*586A>G
NM_001190233.2:c.*586A>G	NP_001177162.1:n.*586A>G
NR_033721.2:n.1019A>G
NR_033722.2:n.991A>G