Canonical Allele Identifier: CA8919820
Gene: HRH4 HGNC NCBI

Linked Data

dbSNP Id: rs150102935

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476889G>A , CM000680.2:g.24476889G>A GRCh38
NC_000018.9:g.22056853G>A , CM000680.1:g.22056853G>A GRCh37
NC_000018.8:g.20310851G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.500G>A MANE Select ENSP00000256906.4:p.Gly167Glu
ENST00000256906.4:c.500G>A ENSP00000256906.4:p.Gly167Glu
ENST00000426880.2:c.236G>A ENSP00000402526.2:p.Gly79Glu
NM_001143828.1:c.236G>A NP_001137300.1:p.Gly79Glu
NM_001160166.1:c.*132G>A NP_001153638.1:n.*132G>A
NM_021624.3:c.500G>A NP_067637.2:p.Gly167Glu
XM_011526133.1:c.357+7938G>A XP_011524435.1:n.357+7938G>A
NM_021624.4:c.500G>A MANE Select NP_067637.2:p.Gly167Glu
NM_001143828.2:c.236G>A NP_001137300.1:p.Gly79Glu
NM_001160166.2:c.*132G>A NP_001153638.1:n.*132G>A