Canonical Allele Identifier: CA1365504729

Gene: CHDH

Linked Data

• dbSNP Id: rs922757788

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.53844927C>A , CM000665.2:g.53844927C>A	GRCh38
NC_000003.11:g.53878954C>A , CM000665.1:g.53878954C>A	GRCh37
NC_000003.10:g.53853994C>A	NCBI36
NG_028042.1:g.6467G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315251.11:c.-131+1156G>T MANE Select	ENSP00000319851.5:n.-131+1156G>T
ENST00000315251.10:c.-131+1156G>T	ENSP00000319851.5:n.-131+1156G>T
NM_018397.4:c.-131+1156G>T	NP_060867.2:n.-131+1156G>T
XM_006713250.2:c.-131+1156G>T	XP_006713313.1:n.-131+1156G>T
XM_006713251.2:c.-131+895G>T	XP_006713314.1:n.-131+895G>T
XM_006713252.2:c.-131+1156G>T	XP_006713315.1:n.-131+1156G>T
XM_011533939.1:c.-215G>T	XP_011532241.1:n.-215G>T
XM_006713250.4:c.-131+1156G>T	XP_006713313.1:n.-131+1156G>T
XM_006713251.4:c.-131+895G>T	XP_006713314.1:n.-131+895G>T
XM_006713252.4:c.-131+1156G>T	XP_006713315.1:n.-131+1156G>T
XM_011533939.3:c.-215G>T	XP_011532241.1:n.-215G>T
XM_017006799.2:c.-131+1156G>T	XP_016862288.1:n.-131+1156G>T
XR_001740199.2:n.382+1156G>T
XR_002959545.1:n.382+1156G>T
NM_018397.5:c.-131+1156G>T MANE Select	NP_060867.2:n.-131+1156G>T