Canonical Allele Identifier: CA350648273

Gene: DNAJB2

Linked Data

• MyVariant Identifiers: chr2:g.220146758T>G (hg19) ; chr2:g.219282036T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219282036T>G , CM000664.2:g.219282036T>G	GRCh38
NC_000002.11:g.220146758T>G , CM000664.1:g.220146758T>G	GRCh37
NC_000002.10:g.219855002T>G	NCBI36
NG_029553.1:g.7719T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683651.1:n.1030T>G
ENST00000684599.1:n.534T>G
ENST00000336576.10:c.327T>G MANE Select	ENSP00000338019.5:p.Ser109Arg
ENST00000336576.9:c.327T>G	ENSP00000338019.5:p.Ser109Arg
ENST00000392086.8:c.327T>G	ENSP00000375936.4:p.Ser109Arg
ENST00000392087.6:c.327T>G	ENSP00000375937.2:p.Ser109Arg
ENST00000421532.5:c.327T>G	ENSP00000395173.1:p.Ser109Arg
ENST00000425450.5:c.327T>G	ENSP00000414796.1:p.Ser109Arg
ENST00000439026.1:c.327T>G	ENSP00000387951.1:p.Ser109Arg
ENST00000442681.5:c.327T>G	ENSP00000392790.1:p.Ser109Arg
ENST00000463463.5:n.318T>G
ENST00000477917.5:n.1545T>G
ENST00000480537.5:n.515T>G
ENST00000487855.1:n.227T>G
NM_001039550.1:c.327T>G	NP_001034639.1:p.Ser109Arg
NM_006736.5:c.327T>G	NP_006727.2:p.Ser109Arg
NM_001039550.2:c.327T>G	NP_001034639.1:p.Ser109Arg
NM_006736.6:c.327T>G MANE Select	NP_006727.2:p.Ser109Arg