Canonical Allele Identifier: CA89106298

Gene: DNAJC19

Linked Data

• dbSNP Id: rs1035336239
• gnomAD v3: 3-180984057-T-G
• gnomAD v4: 3-180984057-T-G
• MyVariant Identifiers: chr3:g.180701845T>G (hg19) ; chr3:g.180984057T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180984057T>G , CM000665.2:g.180984057T>G	GRCh38
NC_000003.11:g.180701845T>G , CM000665.1:g.180701845T>G	GRCh37
NC_000003.10:g.182184539T>G	NCBI36
NG_022933.1:g.10718A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482363.2:n.3047A>C
ENST00000688055.1:c.*1861A>C	ENSP00000508688.1:n.*1861A>C
ENST00000382564.8:c.*583A>C MANE Select	ENSP00000372005.2:n.*583A>C
ENST00000382564.6:c.*583A>C	ENSP00000372005.2:n.*583A>C
ENST00000469657.5:c.*710A>C	ENSP00000418058.1:n.*710A>C
NM_001190233.1:c.*583A>C	NP_001177162.1:n.*583A>C
NM_145261.3:c.*583A>C	NP_660304.1:n.*583A>C
NR_033721.1:n.1054A>C
NR_033722.1:n.1026A>C
NR_033723.1:n.1051A>C
NR_046073.1:n.900A>C
NM_145261.4:c.*583A>C MANE Select	NP_660304.1:n.*583A>C
NM_001190233.2:c.*583A>C	NP_001177162.1:n.*583A>C
NR_033721.2:n.1016A>C
NR_033722.2:n.988A>C