Canonical Allele Identifier: CA777784911
Gene: HRH4 HGNC NCBI

Linked Data

dbSNP Id: rs1313413395
gnomAD v3: 18-24460613-CAG-C
gnomAD v4: 18-24460613-CAG-C
MyVariant Identifiers: chr18:g.22040578_22040579del (hg19) chr18:g.24460614_24460615del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24460614_24460615del , CM000680.2:g.24460614_24460615del GRCh38
NC_000018.9:g.22040578_22040579del , CM000680.1:g.22040578_22040579del GRCh37
NC_000018.8:g.20294576_20294577del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011526133.1:c.-115_-114del XP_011524435.1:n.-115_-114del
XM_011526134.1:c.-115_-114del XP_011524436.1:n.-115_-114del
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