Canonical Allele Identifier: CA350648332

Gene: DNAJB2

Linked Data

• MyVariant Identifiers: chr2:g.220146769T>C (hg19) ; chr2:g.219282047T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219282047T>C , CM000664.2:g.219282047T>C	GRCh38
NC_000002.11:g.220146769T>C , CM000664.1:g.220146769T>C	GRCh37
NC_000002.10:g.219855013T>C	NCBI36
NG_029553.1:g.7730T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683651.1:n.1041T>C
ENST00000684599.1:n.545T>C
ENST00000336576.10:c.338T>C MANE Select	ENSP00000338019.5:p.Phe113Ser
ENST00000336576.9:c.338T>C	ENSP00000338019.5:p.Phe113Ser
ENST00000392086.8:c.338T>C	ENSP00000375936.4:p.Phe113Ser
ENST00000392087.6:c.338T>C	ENSP00000375937.2:p.Phe113Ser
ENST00000421532.5:c.338T>C	ENSP00000395173.1:p.Phe113Ser
ENST00000425450.5:c.338T>C	ENSP00000414796.1:p.Phe113Ser
ENST00000439026.1:c.338T>C	ENSP00000387951.1:p.Phe113Ser
ENST00000442681.5:c.338T>C	ENSP00000392790.1:p.Phe113Ser
ENST00000463463.5:n.329T>C
ENST00000477917.5:n.1556T>C
ENST00000480537.5:n.526T>C
ENST00000487855.1:n.238T>C
NM_001039550.1:c.338T>C	NP_001034639.1:p.Phe113Ser
NM_006736.5:c.338T>C	NP_006727.2:p.Phe113Ser
NM_001039550.2:c.338T>C	NP_001034639.1:p.Phe113Ser
NM_006736.6:c.338T>C MANE Select	NP_006727.2:p.Phe113Ser