Canonical Allele Identifier: CA2290572979

Gene: HRH4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24466692C= , CM000680.2:g.24466692C=	GRCh38
NC_000018.9:g.22046656C= , CM000680.1:g.22046656C=	GRCh37
NC_000018.8:g.20300654C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_021624.4:c.194-2096C= MANE Select	NP_067637.2:n.194-2096C=
ENST00000256906.5:c.194-2096C= MANE Select	ENSP00000256906.4:n.194-2096C=
NM_001143828.1:c.193+5771C=	NP_001137300.1:n.193+5771C=
NM_001143828.2:c.193+5771C=	NP_001137300.1:n.193+5771C=
NM_001160166.1:c.193+5771C=	NP_001153638.1:n.193+5771C=
NM_001160166.2:c.193+5771C=	NP_001153638.1:n.193+5771C=
NM_021624.3:c.194-2096C=	NP_067637.2:n.194-2096C=
ENST00000256906.4:c.194-2096C=	ENSP00000256906.4:n.194-2096C=
ENST00000426880.2:c.193+5771C=	ENSP00000402526.2:n.193+5771C=
XM_011526133.1:c.194-2096C=	XP_011524435.1:n.194-2096C=
XM_011526134.1:c.194-2096C=	XP_011524436.1:n.194-2096C=