Canonical Allele Identifier: CA350648284

Gene: DNAJB2

Linked Data

• MyVariant Identifiers: chr2:g.220146760G>C (hg19) ; chr2:g.219282038G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219282038G>C , CM000664.2:g.219282038G>C	GRCh38
NC_000002.11:g.220146760G>C , CM000664.1:g.220146760G>C	GRCh37
NC_000002.10:g.219855004G>C	NCBI36
NG_029553.1:g.7721G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683651.1:n.1032G>C
ENST00000684599.1:n.536G>C
ENST00000336576.10:c.329G>C MANE Select	ENSP00000338019.5:p.Gly110Ala
ENST00000336576.9:c.329G>C	ENSP00000338019.5:p.Gly110Ala
ENST00000392086.8:c.329G>C	ENSP00000375936.4:p.Gly110Ala
ENST00000392087.6:c.329G>C	ENSP00000375937.2:p.Gly110Ala
ENST00000421532.5:c.329G>C	ENSP00000395173.1:p.Gly110Ala
ENST00000425450.5:c.329G>C	ENSP00000414796.1:p.Gly110Ala
ENST00000439026.1:c.329G>C	ENSP00000387951.1:p.Gly110Ala
ENST00000442681.5:c.329G>C	ENSP00000392790.1:p.Gly110Ala
ENST00000463463.5:n.320G>C
ENST00000477917.5:n.1547G>C
ENST00000480537.5:n.517G>C
ENST00000487855.1:n.229G>C
NM_001039550.1:c.329G>C	NP_001034639.1:p.Gly110Ala
NM_006736.5:c.329G>C	NP_006727.2:p.Gly110Ala
NM_001039550.2:c.329G>C	NP_001034639.1:p.Gly110Ala
NM_006736.6:c.329G>C MANE Select	NP_006727.2:p.Gly110Ala