Canonical Allele Identifier: CA387226007

Gene: DHX37

Linked Data

• dbSNP Id: rs1363738009
• gnomAD v3: 12-124968600-G-T
• gnomAD v4: 12-124968600-G-T
• MyVariant Identifiers: chr12:g.125453146G>T (hg19) ; chr12:g.124968600G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968600G>T , CM000674.2:g.124968600G>T	GRCh38
NC_000012.11:g.125453146G>T , CM000674.1:g.125453146G>T	GRCh37
NC_000012.10:g.124019099G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308736.7:c.1342C>A MANE Select	ENSP00000311135.2:p.Pro448Thr
ENST00000544745.2:c.813C>A
ENST00000679875.1:n.1414C>A
ENST00000308736.6:c.1342C>A	ENSP00000311135.2:p.Pro448Thr
ENST00000539298.1:n.1442C>A
ENST00000544745.1:c.703C>A	ENSP00000439009.1:p.Pro235Thr
NM_032656.3:c.1342C>A	NP_116045.2:p.Pro448Thr
XM_005253590.2:c.1342C>A	XP_005253647.1:p.Pro448Thr
XM_011538597.1:c.1342C>A	XP_011536899.1:p.Pro448Thr
XM_011538598.1:c.1342C>A	XP_011536900.1:p.Pro448Thr
XM_011538599.1:c.1342C>A	XP_011536901.1:p.Pro448Thr
XM_011538600.1:c.1342C>A	XP_011536902.1:p.Pro448Thr
XM_005253590.3:c.1342C>A	XP_005253647.1:p.Pro448Thr
XM_011538598.2:c.1342C>A	XP_011536900.1:p.Pro448Thr
XM_011538600.2:c.1342C>A	XP_011536902.1:p.Pro448Thr
XR_001748819.1:n.1445C>A
XR_001748820.1:n.1445C>A
NM_032656.4:c.1342C>A MANE Select	NP_116045.2:p.Pro448Thr