Canonical Allele Identifier: CA2290577544
Gene: HRH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476773G= , CM000680.2:g.24476773G= GRCh38
NC_000018.9:g.22056737G= , CM000680.1:g.22056737G= GRCh37
NC_000018.8:g.20310735G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.384G= MANE Select ENSP00000256906.4:p.Gly128=
ENST00000256906.4:c.384G= ENSP00000256906.4:p.Gly128=
ENST00000426880.2:c.194-74G= ENSP00000402526.2:n.194-74G=
NM_001143828.1:c.194-74G= NP_001137300.1:n.194-74G=
NM_001160166.1:c.*16G= NP_001153638.1:n.*16G=
NM_021624.3:c.384G= NP_067637.2:p.Gly128=
XM_011526133.1:c.357+7822G= XP_011524435.1:n.357+7822G=
NM_021624.4:c.384G= MANE Select NP_067637.2:p.Gly128=
NM_001143828.2:c.194-74G= NP_001137300.1:n.194-74G=
NM_001160166.2:c.*16G= NP_001153638.1:n.*16G=