Canonical Allele Identifier: CA8919794

Gene: HRH4

Linked Data

• dbSNP Id: rs759077481
• ExAC: 18:22056710 G / A
• gnomAD v2: 18-22056710-G-A
• gnomAD v4: 18-24476746-G-A
• MyVariant Identifiers: chr18:g.22056710G>A (hg19) ; chr18:g.24476746G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476746G>A , CM000680.2:g.24476746G>A	GRCh38
NC_000018.9:g.22056710G>A , CM000680.1:g.22056710G>A	GRCh37
NC_000018.8:g.20310708G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.358-1G>A MANE Select	ENSP00000256906.4:n.358-1G>A
ENST00000256906.4:c.358-1G>A	ENSP00000256906.4:n.358-1G>A
ENST00000426880.2:c.194-101G>A	ENSP00000402526.2:n.194-101G>A
NM_001143828.1:c.194-101G>A	NP_001137300.1:n.194-101G>A
NM_001160166.1:c.194-1G>A	NP_001153638.1:n.194-1G>A
NM_021624.3:c.358-1G>A	NP_067637.2:n.358-1G>A
XM_011526133.1:c.357+7795G>A	XP_011524435.1:n.357+7795G>A
NM_021624.4:c.358-1G>A MANE Select	NP_067637.2:n.358-1G>A
NM_001143828.2:c.194-101G>A	NP_001137300.1:n.194-101G>A
NM_001160166.2:c.194-1G>A	NP_001153638.1:n.194-1G>A