Canonical Allele Identifier: CA2290577682
Gene: HRH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24477092A= , CM000680.2:g.24477092A= GRCh38
NC_000018.9:g.22057056A= , CM000680.1:g.22057056A= GRCh37
NC_000018.8:g.20311054A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.703A= MANE Select ENSP00000256906.4:p.Arg235=
ENST00000256906.4:c.703A= ENSP00000256906.4:p.Arg235=
ENST00000426880.2:c.439A= ENSP00000402526.2:p.Arg147=
NM_001143828.1:c.439A= NP_001137300.1:p.Arg147=
NM_001160166.1:c.*335A= NP_001153638.1:n.*335A=
NM_021624.3:c.703A= NP_067637.2:p.Arg235=
XM_011526133.1:c.357+8141A= XP_011524435.1:n.357+8141A=
NM_021624.4:c.703A= MANE Select NP_067637.2:p.Arg235=
NM_001143828.2:c.439A= NP_001137300.1:p.Arg147=
NM_001160166.2:c.*335A= NP_001153638.1:n.*335A=