Canonical Allele Identifier: CA458781552

Gene: DNAJB6

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.157409916C>T , CM000669.2:g.157409916C>T	GRCh38
NC_000007.13:g.157202610C>T , CM000669.1:g.157202610C>T	GRCh37
NC_000007.12:g.156895371C>T	NCBI36
NG_032573.1:g.77901C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262177.9:c.813C>T MANE Select	ENSP00000262177.4:p.His271=
ENST00000262177.8:c.813C>T	ENSP00000262177.4:p.His271=
ENST00000443280.5:c.468C>T	ENSP00000396267.1:p.His156=
ENST00000459889.5:c.813C>T	ENSP00000488263.1:p.His271=
ENST00000465908.5:n.609C>T
ENST00000634080.1:c.813C>T	ENSP00000488740.1:p.His271=
NM_058246.3:c.813C>T	NP_490647.1:p.His271=
XM_005249515.2:c.813C>T	XP_005249572.1:p.His271=
XM_005249516.2:c.813C>T	XP_005249573.1:p.His271=
XM_006715823.1:c.692-6100C>T	XP_006715886.1:n.692-6100C>T
XM_011515704.1:c.813C>T	XP_011514006.1:p.His271=
NM_001363676.1:c.468C>T	NP_001350605.1:p.His156=
XM_005249515.3:c.813C>T	XP_005249572.1:p.His271=
XM_006715823.2:c.692-6100C>T	XP_006715886.1:n.692-6100C>T
NM_058246.4:c.813C>T MANE Select	NP_490647.1:p.His271=