Canonical Allele Identifier: CA2290577531

Gene: HRH4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476747G= , CM000680.2:g.24476747G=	GRCh38
NC_000018.9:g.22056711G= , CM000680.1:g.22056711G=	GRCh37
NC_000018.8:g.20310709G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.358G= MANE Select	ENSP00000256906.4:p.Val120=
ENST00000256906.4:c.358G=	ENSP00000256906.4:p.Val120=
ENST00000426880.2:c.194-100G=	ENSP00000402526.2:n.194-100G=
NM_001143828.1:c.194-100G=	NP_001137300.1:n.194-100G=
NM_001160166.1:c.194G=	NP_001153638.1:p.Gly65=
NM_021624.3:c.358G=	NP_067637.2:p.Val120=
XM_011526133.1:c.357+7796G=	XP_011524435.1:n.357+7796G=
NM_021624.4:c.358G= MANE Select	NP_067637.2:p.Val120=
NM_001143828.2:c.194-100G=	NP_001137300.1:n.194-100G=
NM_001160166.2:c.194G=	NP_001153638.1:p.Gly65=