Canonical Allele Identifier: CA297158473
Gene: HRH4 HGNC NCBI

Linked Data

dbSNP Id: rs767412017
MyVariant Identifiers: chr18:g.22060859C>A (hg19) chr18:g.24480895C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24480895C>A , CM000680.2:g.24480895C>A GRCh38
NC_000018.9:g.22060859C>A , CM000680.1:g.22060859C>A GRCh37
NC_000018.8:g.20314857C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011526133.1:c.358-5775C>A XP_011524435.1:n.358-5775C>A
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