Canonical Allele Identifier: CA402082831
Gene: HRH4 HGNC NCBI

Linked Data

dbSNP Id: rs1377455216

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476879T>A , CM000680.2:g.24476879T>A GRCh38
NC_000018.9:g.22056843T>A , CM000680.1:g.22056843T>A GRCh37
NC_000018.8:g.20310841T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.490T>A MANE Select ENSP00000256906.4:p.Cys164Ser
ENST00000256906.4:c.490T>A ENSP00000256906.4:p.Cys164Ser
ENST00000426880.2:c.226T>A ENSP00000402526.2:p.Cys76Ser
NM_001143828.1:c.226T>A NP_001137300.1:p.Cys76Ser
NM_001160166.1:c.*122T>A NP_001153638.1:n.*122T>A
NM_021624.3:c.490T>A NP_067637.2:p.Cys164Ser
XM_011526133.1:c.357+7928T>A XP_011524435.1:n.357+7928T>A
NM_021624.4:c.490T>A MANE Select NP_067637.2:p.Cys164Ser
NM_001143828.2:c.226T>A NP_001137300.1:p.Cys76Ser
NM_001160166.2:c.*122T>A NP_001153638.1:n.*122T>A