Canonical Allele Identifier: CA2290577685
Gene: HRH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24477097A= , CM000680.2:g.24477097A= GRCh38
NC_000018.9:g.22057061A= , CM000680.1:g.22057061A= GRCh37
NC_000018.8:g.20311059A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.708A= MANE Select ENSP00000256906.4:p.Arg236=
ENST00000256906.4:c.708A= ENSP00000256906.4:p.Arg236=
ENST00000426880.2:c.444A= ENSP00000402526.2:p.Arg148=
NM_001143828.1:c.444A= NP_001137300.1:p.Arg148=
NM_001160166.1:c.*340A= NP_001153638.1:n.*340A=
NM_021624.3:c.708A= NP_067637.2:p.Arg236=
XM_011526133.1:c.357+8146A= XP_011524435.1:n.357+8146A=
NM_021624.4:c.708A= MANE Select NP_067637.2:p.Arg236=
NM_001143828.2:c.444A= NP_001137300.1:p.Arg148=
NM_001160166.2:c.*340A= NP_001153638.1:n.*340A=