Canonical Allele Identifier: CA350648026
Gene: DNAJB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219281989T>C , CM000664.2:g.219281989T>C GRCh38
NC_000002.11:g.220146711T>C , CM000664.1:g.220146711T>C GRCh37
NC_000002.10:g.219854955T>C NCBI36
NG_029553.1:g.7672T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000683651.1:n.983T>C
ENST00000684599.1:n.487T>C
ENST00000336576.10:c.280T>C MANE Select ENSP00000338019.5:p.Phe94Leu
ENST00000336576.9:c.280T>C ENSP00000338019.5:p.Phe94Leu
ENST00000392086.8:c.280T>C ENSP00000375936.4:p.Phe94Leu
ENST00000392087.6:c.280T>C ENSP00000375937.2:p.Phe94Leu
ENST00000421532.5:c.280T>C ENSP00000395173.1:p.Phe94Leu
ENST00000425450.5:c.280T>C ENSP00000414796.1:p.Phe94Leu
ENST00000439026.1:c.280T>C ENSP00000387951.1:p.Phe94Leu
ENST00000442681.5:c.280T>C ENSP00000392790.1:p.Phe94Leu
ENST00000463463.5:n.271T>C
ENST00000477917.5:n.1498T>C
ENST00000480537.5:n.468T>C
ENST00000487855.1:n.180T>C
NM_001039550.1:c.280T>C NP_001034639.1:p.Phe94Leu
NM_006736.5:c.280T>C NP_006727.2:p.Phe94Leu
NM_001039550.2:c.280T>C NP_001034639.1:p.Phe94Leu
NM_006736.6:c.280T>C MANE Select NP_006727.2:p.Phe94Leu