Canonical Allele Identifier: CA628689357

Gene: HRH4

Linked Data

• dbSNP Id: rs1157160459
• gnomAD v2: 18-22040584-G-A
• gnomAD v3: 18-24460620-G-A
• gnomAD v4: 18-24460620-G-A
• MyVariant Identifiers: chr18:g.22040584G>A (hg19) ; chr18:g.24460620G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24460620G>A , CM000680.2:g.24460620G>A	GRCh38
NC_000018.9:g.22040584G>A , CM000680.1:g.22040584G>A	GRCh37
NC_000018.8:g.20294582G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011526133.1:c.-109G>A	XP_011524435.1:n.-109G>A
XM_011526134.1:c.-109G>A	XP_011524436.1:n.-109G>A