Canonical Allele Identifier: CA402082863
Gene: HRH4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476893T>G , CM000680.2:g.24476893T>G GRCh38
NC_000018.9:g.22056857T>G , CM000680.1:g.22056857T>G GRCh37
NC_000018.8:g.20310855T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.504T>G MANE Select ENSP00000256906.4:p.Phe168Leu
ENST00000256906.4:c.504T>G ENSP00000256906.4:p.Phe168Leu
ENST00000426880.2:c.240T>G ENSP00000402526.2:p.Phe80Leu
NM_001143828.1:c.240T>G NP_001137300.1:p.Phe80Leu
NM_001160166.1:c.*136T>G NP_001153638.1:n.*136T>G
NM_021624.3:c.504T>G NP_067637.2:p.Phe168Leu
XM_011526133.1:c.357+7942T>G XP_011524435.1:n.357+7942T>G
NM_021624.4:c.504T>G MANE Select NP_067637.2:p.Phe168Leu
NM_001143828.2:c.240T>G NP_001137300.1:p.Phe80Leu
NM_001160166.2:c.*136T>G NP_001153638.1:n.*136T>G