Canonical Allele Identifier: CA65958305
Community Standard Title: NM_006736.6(DNAJB2):c.236G>A (p.Gly79Asp)
Gene: DNAJB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219281945G>A , CM000664.2:g.219281945G>A GRCh38
NC_000002.11:g.220146667G>A , CM000664.1:g.220146667G>A GRCh37
NC_000002.10:g.219854911G>A NCBI36
NG_029553.1:g.7628G>A

Transcript Alleles

HGVS Amino-acid Change
NM_006736.6:c.236G>A MANE Select NP_006727.2:p.Gly79Asp
ENST00000336576.10:c.236G>A MANE Select ENSP00000338019.5:p.Gly79Asp
NM_001039550.1:c.236G>A NP_001034639.1:p.Gly79Asp
NM_001039550.2:c.236G>A NP_001034639.1:p.Gly79Asp
NM_006736.5:c.236G>A NP_006727.2:p.Gly79Asp
ENST00000336576.9:c.236G>A ENSP00000338019.5:p.Gly79Asp
ENST00000392086.8:c.236G>A ENSP00000375936.4:p.Gly79Asp
ENST00000392087.6:c.236G>A ENSP00000375937.2:p.Gly79Asp
ENST00000421532.5:c.236G>A ENSP00000395173.1:p.Gly79Asp
ENST00000425450.5:c.236G>A ENSP00000414796.1:p.Gly79Asp
ENST00000439026.1:c.236G>A ENSP00000387951.1:p.Gly79Asp
ENST00000442681.5:c.236G>A ENSP00000392790.1:p.Gly79Asp
ENST00000463463.5:n.227G>A
ENST00000477917.5:n.1454G>A
ENST00000480537.5:n.424G>A
ENST00000487855.1:n.136G>A
ENST00000683651.1:n.939G>A
ENST00000684599.1:n.443G>A