Canonical Allele Identifier: CA402083103
Gene: HRH4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476999C>A , CM000680.2:g.24476999C>A GRCh38
NC_000018.9:g.22056963C>A , CM000680.1:g.22056963C>A GRCh37
NC_000018.8:g.20310961C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.610C>A MANE Select ENSP00000256906.4:p.Arg204Ser
ENST00000256906.4:c.610C>A ENSP00000256906.4:p.Arg204Ser
ENST00000426880.2:c.346C>A ENSP00000402526.2:p.Arg116Ser
NM_001143828.1:c.346C>A NP_001137300.1:p.Arg116Ser
NM_001160166.1:c.*242C>A NP_001153638.1:n.*242C>A
NM_021624.3:c.610C>A NP_067637.2:p.Arg204Ser
XM_011526133.1:c.357+8048C>A XP_011524435.1:n.357+8048C>A
NM_021624.4:c.610C>A MANE Select NP_067637.2:p.Arg204Ser
NM_001143828.2:c.346C>A NP_001137300.1:p.Arg116Ser
NM_001160166.2:c.*242C>A NP_001153638.1:n.*242C>A