Canonical Allele Identifier: CA387226047

Gene: DHX37

Linked Data

• MyVariant Identifiers: chr12:g.125453164G>C (hg19) ; chr12:g.124968618G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968618G>C , CM000674.2:g.124968618G>C	GRCh38
NC_000012.11:g.125453164G>C , CM000674.1:g.125453164G>C	GRCh37
NC_000012.10:g.124019117G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308736.7:c.1324C>G MANE Select	ENSP00000311135.2:p.His442Asp
ENST00000544745.2:c.795C>G
ENST00000679875.1:n.1396C>G
ENST00000308736.6:c.1324C>G	ENSP00000311135.2:p.His442Asp
ENST00000539298.1:n.1424C>G
ENST00000544745.1:c.685C>G	ENSP00000439009.1:p.His229Asp
NM_032656.3:c.1324C>G	NP_116045.2:p.His442Asp
XM_005253590.2:c.1324C>G	XP_005253647.1:p.His442Asp
XM_011538597.1:c.1324C>G	XP_011536899.1:p.His442Asp
XM_011538598.1:c.1324C>G	XP_011536900.1:p.His442Asp
XM_011538599.1:c.1324C>G	XP_011536901.1:p.His442Asp
XM_011538600.1:c.1324C>G	XP_011536902.1:p.His442Asp
XM_005253590.3:c.1324C>G	XP_005253647.1:p.His442Asp
XM_011538598.2:c.1324C>G	XP_011536900.1:p.His442Asp
XM_011538600.2:c.1324C>G	XP_011536902.1:p.His442Asp
XR_001748819.1:n.1427C>G
XR_001748820.1:n.1427C>G
NM_032656.4:c.1324C>G MANE Select	NP_116045.2:p.His442Asp