Canonical Allele Identifier: CA297158456
Gene: HRH4 HGNC NCBI

Linked Data

dbSNP Id: rs1036872663
gnomAD v3: 18-24480887-T-C
gnomAD v4: 18-24480887-T-C
MyVariant Identifiers: chr18:g.22060851T>C (hg19) chr18:g.24480887T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24480887T>C , CM000680.2:g.24480887T>C GRCh38
NC_000018.9:g.22060851T>C , CM000680.1:g.22060851T>C GRCh37
NC_000018.8:g.20314849T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011526133.1:c.358-5783T>C XP_011524435.1:n.358-5783T>C
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