Canonical Allele Identifier: CA8919791

Gene: HRH4

Linked Data

• dbSNP Id: rs111562857
• ExAC: 18:22056683 A / G
• gnomAD v2: 18-22056683-A-G
• gnomAD v3: 18-24476719-A-G
• gnomAD v4: 18-24476719-A-G
• MyVariant Identifiers: chr18:g.22056683A>G (hg19) ; chr18:g.24476719A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476719A>G , CM000680.2:g.24476719A>G	GRCh38
NC_000018.9:g.22056683A>G , CM000680.1:g.22056683A>G	GRCh37
NC_000018.8:g.20310681A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000256906.5:c.358-28A>G MANE Select	ENSP00000256906.4:n.358-28A>G
ENST00000256906.4:c.358-28A>G	ENSP00000256906.4:n.358-28A>G
ENST00000426880.2:c.194-128A>G	ENSP00000402526.2:n.194-128A>G
NM_001143828.1:c.194-128A>G	NP_001137300.1:n.194-128A>G
NM_001160166.1:c.194-28A>G	NP_001153638.1:n.194-28A>G
NM_021624.3:c.358-28A>G	NP_067637.2:n.358-28A>G
XM_011526133.1:c.357+7768A>G	XP_011524435.1:n.357+7768A>G
NM_021624.4:c.358-28A>G MANE Select	NP_067637.2:n.358-28A>G
NM_001143828.2:c.194-128A>G	NP_001137300.1:n.194-128A>G
NM_001160166.2:c.194-28A>G	NP_001153638.1:n.194-28A>G