Canonical Allele Identifier: CA297158417
Gene: HRH4 HGNC NCBI

Linked Data

dbSNP Id: rs920972067
gnomAD v3: 18-24480867-C-T
gnomAD v4: 18-24480867-C-T
COSMIC: COSN16943426
MyVariant Identifiers: chr18:g.22060831C>T (hg19) chr18:g.24480867C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24480867C>T , CM000680.2:g.24480867C>T GRCh38
NC_000018.9:g.22060831C>T , CM000680.1:g.22060831C>T GRCh37
NC_000018.8:g.20314829C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011526133.1:c.358-5803C>T XP_011524435.1:n.358-5803C>T
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Search 100 bp 3'