Canonical Allele Identifier: CA402082673
Gene: HRH4 HGNC NCBI

Linked Data

dbSNP Id: rs953437853
gnomAD v3: 18-24476810-G-A
gnomAD v4: 18-24476810-G-A
MyVariant Identifiers: chr18:g.22056774G>A (hg19) chr18:g.24476810G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476810G>A , CM000680.2:g.24476810G>A GRCh38
NC_000018.9:g.22056774G>A , CM000680.1:g.22056774G>A GRCh37
NC_000018.8:g.20310772G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000256906.5:c.421G>A MANE Select ENSP00000256906.4:p.Val141Met
ENST00000256906.4:c.421G>A ENSP00000256906.4:p.Val141Met
ENST00000426880.2:c.194-37G>A ENSP00000402526.2:n.194-37G>A
NM_001143828.1:c.194-37G>A NP_001137300.1:n.194-37G>A
NM_001160166.1:c.*53G>A NP_001153638.1:n.*53G>A
NM_021624.3:c.421G>A NP_067637.2:p.Val141Met
XM_011526133.1:c.357+7859G>A XP_011524435.1:n.357+7859G>A
NM_021624.4:c.421G>A MANE Select NP_067637.2:p.Val141Met
NM_001143828.2:c.194-37G>A NP_001137300.1:n.194-37G>A
NM_001160166.2:c.*53G>A NP_001153638.1:n.*53G>A
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