Canonical Allele Identifier: CA777784903

Gene: HRH4

Linked Data

• dbSNP Id: rs1255049269
• gnomAD v3: 18-24460590-A-G
• gnomAD v4: 18-24460590-A-G
• MyVariant Identifiers: chr18:g.22040554A>G (hg19) ; chr18:g.24460590A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24460590A>G , CM000680.2:g.24460590A>G	GRCh38
NC_000018.9:g.22040554A>G , CM000680.1:g.22040554A>G	GRCh37
NC_000018.8:g.20294552A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011526133.1:c.-139A>G	XP_011524435.1:n.-139A>G
XM_011526134.1:c.-139A>G	XP_011524436.1:n.-139A>G