Canonical Allele Identifier: CA6872021
Gene: DHX37 HGNC NCBI

Linked Data

ClinVar Variation Id: 402138
dbSNP Id: rs779613772

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.124967167C>T , CM000674.2:g.124967167C>T GRCh38
NC_000012.11:g.125451713C>T , CM000674.1:g.125451713C>T GRCh37
NC_000012.10:g.124017666C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000308736.7:c.1460G>A MANE Select ENSP00000311135.2:p.Arg487His
ENST00000544745.2:c.931G>A
ENST00000679875.1:n.1532G>A
ENST00000308736.6:c.1460G>A ENSP00000311135.2:p.Arg487His
ENST00000539298.1:n.1560G>A
ENST00000544745.1:c.821G>A ENSP00000439009.1:p.Arg274His
NM_032656.3:c.1460G>A NP_116045.2:p.Arg487His
XM_005253590.2:c.1460G>A XP_005253647.1:p.Arg487His
XM_011538597.1:c.1460G>A XP_011536899.1:p.Arg487His
XM_011538598.1:c.1460G>A XP_011536900.1:p.Arg487His
XM_011538599.1:c.1460G>A XP_011536901.1:p.Arg487His
XM_011538600.1:c.1460G>A XP_011536902.1:p.Arg487His
XM_005253590.3:c.1460G>A XP_005253647.1:p.Arg487His
XM_011538598.2:c.1460G>A XP_011536900.1:p.Arg487His
XM_011538600.2:c.1460G>A XP_011536902.1:p.Arg487His
XR_001748819.1:n.1563G>A
XR_001748820.1:n.1563G>A
NM_032656.4:c.1460G>A MANE Select NP_116045.2:p.Arg487His