Canonical Allele Identifier: CA952910134

Gene: DHX37

Linked Data

• dbSNP Id: rs1954452809
• gnomAD v3: 12-124968785-A-C
• gnomAD v4: 12-124968785-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968785A>C , CM000674.2:g.124968785A>C	GRCh38
NC_000012.11:g.125453331A>C , CM000674.1:g.125453331A>C	GRCh37
NC_000012.10:g.124019284A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308736.7:c.1293+82T>G MANE Select	ENSP00000311135.2:n.1293+82T>G
ENST00000544745.2:c.764+82T>G
ENST00000679875.1:n.1365+82T>G
ENST00000308736.6:c.1293+82T>G	ENSP00000311135.2:n.1293+82T>G
ENST00000539298.1:n.1393+82T>G
ENST00000544745.1:c.654+82T>G	ENSP00000439009.1:n.654+82T>G
NM_032656.3:c.1293+82T>G	NP_116045.2:n.1293+82T>G
XM_005253590.2:c.1293+82T>G	XP_005253647.1:n.1293+82T>G
XM_011538597.1:c.1293+82T>G	XP_011536899.1:n.1293+82T>G
XM_011538598.1:c.1293+82T>G	XP_011536900.1:n.1293+82T>G
XM_011538599.1:c.1293+82T>G	XP_011536901.1:n.1293+82T>G
XM_011538600.1:c.1293+82T>G	XP_011536902.1:n.1293+82T>G
XM_005253590.3:c.1293+82T>G	XP_005253647.1:n.1293+82T>G
XM_011538598.2:c.1293+82T>G	XP_011536900.1:n.1293+82T>G
XM_011538600.2:c.1293+82T>G	XP_011536902.1:n.1293+82T>G
XR_001748819.1:n.1396+82T>G
XR_001748820.1:n.1396+82T>G
NM_032656.4:c.1293+82T>G MANE Select	NP_116045.2:n.1293+82T>G