Canonical Allele Identifier: CA350648226

Gene: DNAJB2

Linked Data

• MyVariant Identifiers: chr2:g.220146750T>A (hg19) ; chr2:g.219282028T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219282028T>A , CM000664.2:g.219282028T>A	GRCh38
NC_000002.11:g.220146750T>A , CM000664.1:g.220146750T>A	GRCh37
NC_000002.10:g.219854994T>A	NCBI36
NG_029553.1:g.7711T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683651.1:n.1022T>A
ENST00000684599.1:n.526T>A
ENST00000336576.10:c.319T>A MANE Select	ENSP00000338019.5:p.Phe107Ile
ENST00000336576.9:c.319T>A	ENSP00000338019.5:p.Phe107Ile
ENST00000392086.8:c.319T>A	ENSP00000375936.4:p.Phe107Ile
ENST00000392087.6:c.319T>A	ENSP00000375937.2:p.Phe107Ile
ENST00000421532.5:c.319T>A	ENSP00000395173.1:p.Phe107Ile
ENST00000425450.5:c.319T>A	ENSP00000414796.1:p.Phe107Ile
ENST00000439026.1:c.319T>A	ENSP00000387951.1:p.Phe107Ile
ENST00000442681.5:c.319T>A	ENSP00000392790.1:p.Phe107Ile
ENST00000463463.5:n.310T>A
ENST00000477917.5:n.1537T>A
ENST00000480537.5:n.507T>A
ENST00000487855.1:n.219T>A
NM_001039550.1:c.319T>A	NP_001034639.1:p.Phe107Ile
NM_006736.5:c.319T>A	NP_006727.2:p.Phe107Ile
NM_001039550.2:c.319T>A	NP_001034639.1:p.Phe107Ile
NM_006736.6:c.319T>A MANE Select	NP_006727.2:p.Phe107Ile