Canonical Allele Identifier: CA482291549

Gene: DHX37

Linked Data

• gnomAD v4: 12-124968873-G-T
• MyVariant Identifiers: chr12:g.125453419G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968873G>T , CM000674.2:g.124968873G>T	GRCh38
NC_000012.11:g.125453419G>T , CM000674.1:g.125453419G>T	GRCh37
NC_000012.10:g.124019372G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308736.7:c.1287C>A MANE Select	ENSP00000311135.2:p.Val429=
ENST00000544745.2:c.758C>A
ENST00000679875.1:n.1359C>A
ENST00000308736.6:c.1287C>A	ENSP00000311135.2:p.Val429=
ENST00000539298.1:n.1387C>A
ENST00000544745.1:c.648C>A	ENSP00000439009.1:p.Val216=
NM_032656.3:c.1287C>A	NP_116045.2:p.Val429=
XM_005253590.2:c.1287C>A	XP_005253647.1:p.Val429=
XM_011538597.1:c.1287C>A	XP_011536899.1:p.Val429=
XM_011538598.1:c.1287C>A	XP_011536900.1:p.Val429=
XM_011538599.1:c.1287C>A	XP_011536901.1:p.Val429=
XM_011538600.1:c.1287C>A	XP_011536902.1:p.Val429=
XM_005253590.3:c.1287C>A	XP_005253647.1:p.Val429=
XM_011538598.2:c.1287C>A	XP_011536900.1:p.Val429=
XM_011538600.2:c.1287C>A	XP_011536902.1:p.Val429=
XR_001748819.1:n.1390C>A
XR_001748820.1:n.1390C>A
NM_032656.4:c.1287C>A MANE Select	NP_116045.2:p.Val429=