Canonical Allele Identifier: CA482291586

Gene: DHX37

Linked Data

• MyVariant Identifiers: chr12:g.125453476C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968930C>G , CM000674.2:g.124968930C>G	GRCh38
NC_000012.11:g.125453476C>G , CM000674.1:g.125453476C>G	GRCh37
NC_000012.10:g.124019429C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308736.7:c.1230G>C MANE Select	ENSP00000311135.2:p.Thr410=
ENST00000544745.2:c.701G>C
ENST00000679875.1:n.1302G>C
ENST00000308736.6:c.1230G>C	ENSP00000311135.2:p.Thr410=
ENST00000539298.1:n.1330G>C
ENST00000544745.1:c.591G>C	ENSP00000439009.1:p.Thr197=
NM_032656.3:c.1230G>C	NP_116045.2:p.Thr410=
XM_005253590.2:c.1230G>C	XP_005253647.1:p.Thr410=
XM_011538597.1:c.1230G>C	XP_011536899.1:p.Thr410=
XM_011538598.1:c.1230G>C	XP_011536900.1:p.Thr410=
XM_011538599.1:c.1230G>C	XP_011536901.1:p.Thr410=
XM_011538600.1:c.1230G>C	XP_011536902.1:p.Thr410=
XM_005253590.3:c.1230G>C	XP_005253647.1:p.Thr410=
XM_011538598.2:c.1230G>C	XP_011536900.1:p.Thr410=
XM_011538600.2:c.1230G>C	XP_011536902.1:p.Thr410=
XR_001748819.1:n.1333G>C
XR_001748820.1:n.1333G>C
NM_032656.4:c.1230G>C MANE Select	NP_116045.2:p.Thr410=