Canonical Allele Identifier: CA431268280
Gene: DNAJB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.220146761A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219282039A>G , CM000664.2:g.219282039A>G GRCh38
NC_000002.11:g.220146761A>G , CM000664.1:g.220146761A>G GRCh37
NC_000002.10:g.219855005A>G NCBI36
NG_029553.1:g.7722A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000683651.1:n.1033A>G
ENST00000684599.1:n.537A>G
ENST00000336576.10:c.330A>G MANE Select ENSP00000338019.5:p.Gly110=
ENST00000336576.9:c.330A>G ENSP00000338019.5:p.Gly110=
ENST00000392086.8:c.330A>G ENSP00000375936.4:p.Gly110=
ENST00000392087.6:c.330A>G ENSP00000375937.2:p.Gly110=
ENST00000421532.5:c.330A>G ENSP00000395173.1:p.Gly110=
ENST00000425450.5:c.330A>G ENSP00000414796.1:p.Gly110=
ENST00000439026.1:c.330A>G ENSP00000387951.1:p.Gly110=
ENST00000442681.5:c.330A>G ENSP00000392790.1:p.Gly110=
ENST00000463463.5:n.321A>G
ENST00000477917.5:n.1548A>G
ENST00000480537.5:n.518A>G
ENST00000487855.1:n.230A>G
NM_001039550.1:c.330A>G NP_001034639.1:p.Gly110=
NM_006736.5:c.330A>G NP_006727.2:p.Gly110=
NM_001039550.2:c.330A>G NP_001034639.1:p.Gly110=
NM_006736.6:c.330A>G MANE Select NP_006727.2:p.Gly110=