Canonical Allele Identifier: CA8919815
Gene: HRH4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3106965
ClinVar RCV Id: RCV004402337
dbSNP Id: rs774932796
ExAC: 18:22056834 G / A
gnomAD v2: 18-22056834-G-A
gnomAD v3: 18-24476870-G-A
gnomAD v4: 18-24476870-G-A
MyVariant Identifiers: chr18:g.22056834G>A (hg19) chr18:g.24476870G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476870G>A , CM000680.2:g.24476870G>A GRCh38
NC_000018.9:g.22056834G>A , CM000680.1:g.22056834G>A GRCh37
NC_000018.8:g.20310832G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.481G>A MANE Select ENSP00000256906.4:p.Gly161Ser
ENST00000256906.4:c.481G>A ENSP00000256906.4:p.Gly161Ser
ENST00000426880.2:c.217G>A ENSP00000402526.2:p.Gly73Ser
NM_001143828.1:c.217G>A NP_001137300.1:p.Gly73Ser
NM_001160166.1:c.*113G>A NP_001153638.1:n.*113G>A
NM_021624.3:c.481G>A NP_067637.2:p.Gly161Ser
XM_011526133.1:c.357+7919G>A XP_011524435.1:n.357+7919G>A
NM_021624.4:c.481G>A MANE Select NP_067637.2:p.Gly161Ser
NM_001143828.2:c.217G>A NP_001137300.1:p.Gly73Ser
NM_001160166.2:c.*113G>A NP_001153638.1:n.*113G>A
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