Canonical Allele Identifier: CA503523573

Gene: HRH4

Linked Data

• dbSNP Id: rs779530887
• gnomAD v3: 18-24477031-T-A
• gnomAD v4: 18-24477031-T-A
• MyVariant Identifiers: chr18:g.22056995T>A (hg19) ; chr18:g.24477031T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24477031T>A , CM000680.2:g.24477031T>A	GRCh38
NC_000018.9:g.22056995T>A , CM000680.1:g.22056995T>A	GRCh37
NC_000018.8:g.20310993T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.642T>A MANE Select	ENSP00000256906.4:p.Pro214=
ENST00000256906.4:c.642T>A	ENSP00000256906.4:p.Pro214=
ENST00000426880.2:c.378T>A	ENSP00000402526.2:p.Pro126=
NM_001143828.1:c.378T>A	NP_001137300.1:p.Pro126=
NM_001160166.1:c.*274T>A	NP_001153638.1:n.*274T>A
NM_021624.3:c.642T>A	NP_067637.2:p.Pro214=
XM_011526133.1:c.357+8080T>A	XP_011524435.1:n.357+8080T>A
NM_021624.4:c.642T>A MANE Select	NP_067637.2:p.Pro214=
NM_001143828.2:c.378T>A	NP_001137300.1:p.Pro126=
NM_001160166.2:c.*274T>A	NP_001153638.1:n.*274T>A