Canonical Allele Identifier: CA777784905
Gene: HRH4 HGNC NCBI

Linked Data

dbSNP Id: rs1207651834
gnomAD v3: 18-24460600-C-T
gnomAD v4: 18-24460600-C-T
MyVariant Identifiers: chr18:g.22040564C>T (hg19) chr18:g.24460600C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24460600C>T , CM000680.2:g.24460600C>T GRCh38
NC_000018.9:g.22040564C>T , CM000680.1:g.22040564C>T GRCh37
NC_000018.8:g.20294562C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011526133.1:c.-129C>T XP_011524435.1:n.-129C>T
XM_011526134.1:c.-129C>T XP_011524436.1:n.-129C>T
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