Canonical Allele Identifier: CA297158421
Gene: HRH4 HGNC NCBI

Linked Data

dbSNP Id: rs932542148
gnomAD v2: 18-22060832-G-A
gnomAD v3: 18-24480868-G-A
gnomAD v4: 18-24480868-G-A
MyVariant Identifiers: chr18:g.22060832G>A (hg19) chr18:g.24480868G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24480868G>A , CM000680.2:g.24480868G>A GRCh38
NC_000018.9:g.22060832G>A , CM000680.1:g.22060832G>A GRCh37
NC_000018.8:g.20314830G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011526133.1:c.358-5802G>A XP_011524435.1:n.358-5802G>A
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