Canonical Allele Identifier: CA2290577618

Gene: HRH4

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476923A= , CM000680.2:g.24476923A=	GRCh38
NC_000018.9:g.22056887A= , CM000680.1:g.22056887A=	GRCh37
NC_000018.8:g.20310885A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.534A= MANE Select	ENSP00000256906.4:p.Thr178=
ENST00000256906.4:c.534A=	ENSP00000256906.4:p.Thr178=
ENST00000426880.2:c.270A=	ENSP00000402526.2:p.Thr90=
NM_001143828.1:c.270A=	NP_001137300.1:p.Thr90=
NM_001160166.1:c.*166A=	NP_001153638.1:n.*166A=
NM_021624.3:c.534A=	NP_067637.2:p.Thr178=
XM_011526133.1:c.357+7972A=	XP_011524435.1:n.357+7972A=
NM_021624.4:c.534A= MANE Select	NP_067637.2:p.Thr178=
NM_001143828.2:c.270A=	NP_001137300.1:p.Thr90=
NM_001160166.2:c.*166A=	NP_001153638.1:n.*166A=