Canonical Allele Identifier: CA2290577741

Gene: HRH4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24477253C= , CM000680.2:g.24477253C=	GRCh38
NC_000018.9:g.22057217C= , CM000680.1:g.22057217C=	GRCh37
NC_000018.8:g.20311215C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.864C= MANE Select	ENSP00000256906.4:p.His288=
ENST00000256906.4:c.864C=	ENSP00000256906.4:p.His288=
ENST00000426880.2:c.600C=	ENSP00000402526.2:p.His200=
NM_001143828.1:c.600C=	NP_001137300.1:p.His200=
NM_001160166.1:c.*496C=	NP_001153638.1:n.*496C=
NM_021624.3:c.864C=	NP_067637.2:p.His288=
XM_011526133.1:c.357+8302C=	XP_011524435.1:n.357+8302C=
NM_021624.4:c.864C= MANE Select	NP_067637.2:p.His288=
NM_001143828.2:c.600C=	NP_001137300.1:p.His200=
NM_001160166.2:c.*496C=	NP_001153638.1:n.*496C=