Canonical Allele Identifier: CA297158452

Gene: HRH4

Linked Data

• dbSNP Id: rs773962113
• gnomAD v3: 18-24480878-C-A
• gnomAD v4: 18-24480878-C-A
• MyVariant Identifiers: chr18:g.22060842C>A (hg19) ; chr18:g.24480878C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24480878C>A , CM000680.2:g.24480878C>A	GRCh38
NC_000018.9:g.22060842C>A , CM000680.1:g.22060842C>A	GRCh37
NC_000018.8:g.20314840C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011526133.1:c.358-5792C>A	XP_011524435.1:n.358-5792C>A