Canonical Allele Identifier: CA777796159

Gene: HRH4

Linked Data

• dbSNP Id: rs1214144946
• gnomAD v3: 18-24480866-C-T
• gnomAD v4: 18-24480866-C-T
• MyVariant Identifiers: chr18:g.22060830C>T (hg19) ; chr18:g.24480866C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24480866C>T , CM000680.2:g.24480866C>T	GRCh38
NC_000018.9:g.22060830C>T , CM000680.1:g.22060830C>T	GRCh37
NC_000018.8:g.20314828C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011526133.1:c.358-5804C>T	XP_011524435.1:n.358-5804C>T