Canonical Allele Identifier: CA2290577532

Gene: HRH4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476748T= , CM000680.2:g.24476748T=	GRCh38
NC_000018.9:g.22056712T= , CM000680.1:g.22056712T=	GRCh37
NC_000018.8:g.20310710T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000256906.5:c.359T= MANE Select	ENSP00000256906.4:p.Val120=
ENST00000256906.4:c.359T=	ENSP00000256906.4:p.Val120=
ENST00000426880.2:c.194-99T=	ENSP00000402526.2:n.194-99T=
NM_001143828.1:c.194-99T=	NP_001137300.1:n.194-99T=
NM_001160166.1:c.195T=	NP_001153638.1:p.Gly65=
NM_021624.3:c.359T=	NP_067637.2:p.Val120=
XM_011526133.1:c.357+7797T=	XP_011524435.1:n.357+7797T=
NM_021624.4:c.359T= MANE Select	NP_067637.2:p.Val120=
NM_001143828.2:c.194-99T=	NP_001137300.1:n.194-99T=
NM_001160166.2:c.195T=	NP_001153638.1:p.Gly65=