Canonical Allele Identifier: CA2290577535

Gene: HRH4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476754A= , CM000680.2:g.24476754A=	GRCh38
NC_000018.9:g.22056718A= , CM000680.1:g.22056718A=	GRCh37
NC_000018.8:g.20310716A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.365A= MANE Select	ENSP00000256906.4:p.Tyr122=
ENST00000256906.4:c.365A=	ENSP00000256906.4:p.Tyr122=
ENST00000426880.2:c.194-93A=	ENSP00000402526.2:n.194-93A=
NM_001143828.1:c.194-93A=	NP_001137300.1:n.194-93A=
NM_001160166.1:c.201A=	NP_001153638.1:p.Leu67=
NM_021624.3:c.365A=	NP_067637.2:p.Tyr122=
XM_011526133.1:c.357+7803A=	XP_011524435.1:n.357+7803A=
NM_021624.4:c.365A= MANE Select	NP_067637.2:p.Tyr122=
NM_001143828.2:c.194-93A=	NP_001137300.1:n.194-93A=
NM_001160166.2:c.201A=	NP_001153638.1:p.Leu67=