Canonical Allele Identifier: CA777796166

Gene: HRH4

Linked Data

• dbSNP Id: rs1274355289
• gnomAD v3: 18-24480876-T-G
• gnomAD v4: 18-24480876-T-G
• MyVariant Identifiers: chr18:g.22060840T>G (hg19) ; chr18:g.24480876T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24480876T>G , CM000680.2:g.24480876T>G	GRCh38
NC_000018.9:g.22060840T>G , CM000680.1:g.22060840T>G	GRCh37
NC_000018.8:g.20314838T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011526133.1:c.358-5794T>G	XP_011524435.1:n.358-5794T>G