Canonical Allele Identifier: CA350648056
Gene: DNAJB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219281993C>G , CM000664.2:g.219281993C>G GRCh38
NC_000002.11:g.220146715C>G , CM000664.1:g.220146715C>G GRCh37
NC_000002.10:g.219854959C>G NCBI36
NG_029553.1:g.7676C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000683651.1:n.987C>G
ENST00000684599.1:n.491C>G
ENST00000336576.10:c.284C>G MANE Select ENSP00000338019.5:p.Thr95Ser
ENST00000336576.9:c.284C>G ENSP00000338019.5:p.Thr95Ser
ENST00000392086.8:c.284C>G ENSP00000375936.4:p.Thr95Ser
ENST00000392087.6:c.284C>G ENSP00000375937.2:p.Thr95Ser
ENST00000421532.5:c.284C>G ENSP00000395173.1:p.Thr95Ser
ENST00000425450.5:c.284C>G ENSP00000414796.1:p.Thr95Ser
ENST00000439026.1:c.284C>G ENSP00000387951.1:p.Thr95Ser
ENST00000442681.5:c.284C>G ENSP00000392790.1:p.Thr95Ser
ENST00000463463.5:n.275C>G
ENST00000477917.5:n.1502C>G
ENST00000480537.5:n.472C>G
ENST00000487855.1:n.184C>G
NM_001039550.1:c.284C>G NP_001034639.1:p.Thr95Ser
NM_006736.5:c.284C>G NP_006727.2:p.Thr95Ser
NM_001039550.2:c.284C>G NP_001034639.1:p.Thr95Ser
NM_006736.6:c.284C>G MANE Select NP_006727.2:p.Thr95Ser