Canonical Allele Identifier: CA431268294

Gene: DNAJB2

Linked Data

• MyVariant Identifiers: chr2:g.220146767T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219282045T>G , CM000664.2:g.219282045T>G	GRCh38
NC_000002.11:g.220146767T>G , CM000664.1:g.220146767T>G	GRCh37
NC_000002.10:g.219855011T>G	NCBI36
NG_029553.1:g.7728T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683651.1:n.1039T>G
ENST00000684599.1:n.543T>G
ENST00000336576.10:c.336T>G MANE Select	ENSP00000338019.5:p.Pro112=
ENST00000336576.9:c.336T>G	ENSP00000338019.5:p.Pro112=
ENST00000392086.8:c.336T>G	ENSP00000375936.4:p.Pro112=
ENST00000392087.6:c.336T>G	ENSP00000375937.2:p.Pro112=
ENST00000421532.5:c.336T>G	ENSP00000395173.1:p.Pro112=
ENST00000425450.5:c.336T>G	ENSP00000414796.1:p.Pro112=
ENST00000439026.1:c.336T>G	ENSP00000387951.1:p.Pro112=
ENST00000442681.5:c.336T>G	ENSP00000392790.1:p.Pro112=
ENST00000463463.5:n.327T>G
ENST00000477917.5:n.1554T>G
ENST00000480537.5:n.524T>G
ENST00000487855.1:n.236T>G
NM_001039550.1:c.336T>G	NP_001034639.1:p.Pro112=
NM_006736.5:c.336T>G	NP_006727.2:p.Pro112=
NM_001039550.2:c.336T>G	NP_001034639.1:p.Pro112=
NM_006736.6:c.336T>G MANE Select	NP_006727.2:p.Pro112=