Canonical Allele Identifier: CA350647854
Gene: DNAJB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219281942C>T , CM000664.2:g.219281942C>T GRCh38
NC_000002.11:g.220146664C>T , CM000664.1:g.220146664C>T GRCh37
NC_000002.10:g.219854908C>T NCBI36
NG_029553.1:g.7625C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000683651.1:n.936C>T
ENST00000684599.1:n.440C>T
ENST00000336576.10:c.233C>T MANE Select ENSP00000338019.5:p.Thr78Ile
ENST00000336576.9:c.233C>T ENSP00000338019.5:p.Thr78Ile
ENST00000392086.8:c.233C>T ENSP00000375936.4:p.Thr78Ile
ENST00000392087.6:c.233C>T ENSP00000375937.2:p.Thr78Ile
ENST00000421532.5:c.233C>T ENSP00000395173.1:p.Thr78Ile
ENST00000425450.5:c.233C>T ENSP00000414796.1:p.Thr78Ile
ENST00000439026.1:c.233C>T ENSP00000387951.1:p.Thr78Ile
ENST00000442681.5:c.233C>T ENSP00000392790.1:p.Thr78Ile
ENST00000463463.5:n.224C>T
ENST00000477917.5:n.1451C>T
ENST00000480537.5:n.421C>T
ENST00000487855.1:n.133C>T
NM_001039550.1:c.233C>T NP_001034639.1:p.Thr78Ile
NM_006736.5:c.233C>T NP_006727.2:p.Thr78Ile
NM_001039550.2:c.233C>T NP_001034639.1:p.Thr78Ile
NM_006736.6:c.233C>T MANE Select NP_006727.2:p.Thr78Ile