Canonical Allele Identifier: CA402082869
Gene: HRH4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476896T>A , CM000680.2:g.24476896T>A GRCh38
NC_000018.9:g.22056860T>A , CM000680.1:g.22056860T>A GRCh37
NC_000018.8:g.20310858T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.507T>A MANE Select ENSP00000256906.4:p.Phe169Leu
ENST00000256906.4:c.507T>A ENSP00000256906.4:p.Phe169Leu
ENST00000426880.2:c.243T>A ENSP00000402526.2:p.Phe81Leu
NM_001143828.1:c.243T>A NP_001137300.1:p.Phe81Leu
NM_001160166.1:c.*139T>A NP_001153638.1:n.*139T>A
NM_021624.3:c.507T>A NP_067637.2:p.Phe169Leu
XM_011526133.1:c.357+7945T>A XP_011524435.1:n.357+7945T>A
NM_021624.4:c.507T>A MANE Select NP_067637.2:p.Phe169Leu
NM_001143828.2:c.243T>A NP_001137300.1:p.Phe81Leu
NM_001160166.2:c.*139T>A NP_001153638.1:n.*139T>A