Canonical Allele Identifier: CA350648122
Gene: DNAJB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219282009G>C , CM000664.2:g.219282009G>C GRCh38
NC_000002.11:g.220146731G>C , CM000664.1:g.220146731G>C GRCh37
NC_000002.10:g.219854975G>C NCBI36
NG_029553.1:g.7692G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000683651.1:n.1003G>C
ENST00000684599.1:n.507G>C
ENST00000336576.10:c.300G>C MANE Select ENSP00000338019.5:p.Glu100Asp
ENST00000336576.9:c.300G>C ENSP00000338019.5:p.Glu100Asp
ENST00000392086.8:c.300G>C ENSP00000375936.4:p.Glu100Asp
ENST00000392087.6:c.300G>C ENSP00000375937.2:p.Glu100Asp
ENST00000421532.5:c.300G>C ENSP00000395173.1:p.Glu100Asp
ENST00000425450.5:c.300G>C ENSP00000414796.1:p.Glu100Asp
ENST00000439026.1:c.300G>C ENSP00000387951.1:p.Glu100Asp
ENST00000442681.5:c.300G>C ENSP00000392790.1:p.Glu100Asp
ENST00000463463.5:n.291G>C
ENST00000477917.5:n.1518G>C
ENST00000480537.5:n.488G>C
ENST00000487855.1:n.200G>C
NM_001039550.1:c.300G>C NP_001034639.1:p.Glu100Asp
NM_006736.5:c.300G>C NP_006727.2:p.Glu100Asp
NM_001039550.2:c.300G>C NP_001034639.1:p.Glu100Asp
NM_006736.6:c.300G>C MANE Select NP_006727.2:p.Glu100Asp