Canonical Allele Identifier: CA65959142
Community Standard Title: NM_006736.6(DNAJB2):c.363C>G (p.Gly121=)
Gene: DNAJB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219282847C>G , CM000664.2:g.219282847C>G GRCh38
NC_000002.11:g.220147569C>G , CM000664.1:g.220147569C>G GRCh37
NC_000002.10:g.219855813C>G NCBI36
NG_029553.1:g.8530C>G

Transcript Alleles

HGVS Amino-acid Change
NM_006736.6:c.363C>G MANE Select NP_006727.2:p.Gly121=
ENST00000336576.10:c.363C>G MANE Select ENSP00000338019.5:p.Gly121=
NM_001039550.1:c.363C>G NP_001034639.1:p.Gly121=
NM_001039550.2:c.363C>G NP_001034639.1:p.Gly121=
NM_006736.5:c.363C>G NP_006727.2:p.Gly121=
ENST00000336576.9:c.363C>G ENSP00000338019.5:p.Gly121=
ENST00000392086.8:c.363C>G ENSP00000375936.4:p.Gly121=
ENST00000392087.6:c.353-286C>G ENSP00000375937.2:n.353-286C>G
ENST00000425450.5:c.363C>G ENSP00000414796.1:p.Gly121=
ENST00000439026.1:c.363C>G ENSP00000387951.1:p.Gly121=
ENST00000442681.5:c.363C>G ENSP00000392790.1:p.Gly121=
ENST00000463463.5:n.354C>G
ENST00000472019.5:n.106C>G
ENST00000473750.5:n.150C>G
ENST00000477917.5:n.1581C>G
ENST00000684599.1:n.570C>G