Canonical Allele Identifier: CA2290570386

Gene: HRH4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24460650A= , CM000680.2:g.24460650A=	GRCh38
NC_000018.9:g.22040614A= , CM000680.1:g.22040614A=	GRCh37
NC_000018.8:g.20294612A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.-79A= MANE Select	ENSP00000256906.4:n.-79A=
ENST00000256906.4:c.-79A=	ENSP00000256906.4:n.-79A=
NM_001143828.1:c.-79A=	NP_001137300.1:n.-79A=
NM_001160166.1:c.-79A=	NP_001153638.1:n.-79A=
NM_021624.3:c.-79A=	NP_067637.2:n.-79A=
XM_011526133.1:c.-79A=	XP_011524435.1:n.-79A=
XM_011526134.1:c.-79A=	XP_011524436.1:n.-79A=
NM_021624.4:c.-79A= MANE Select	NP_067637.2:n.-79A=
NM_001143828.2:c.-79A=	NP_001137300.1:n.-79A=
NM_001160166.2:c.-79A=	NP_001153638.1:n.-79A=