Canonical Allele Identifier: CA503523798

Gene: HRH4

Linked Data

• dbSNP Id: rs1910165808
• gnomAD v3: 18-24477220-T-A
• gnomAD v4: 18-24477220-T-A
• MyVariant Identifiers: chr18:g.22057184T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24477220T>A , CM000680.2:g.24477220T>A	GRCh38
NC_000018.9:g.22057184T>A , CM000680.1:g.22057184T>A	GRCh37
NC_000018.8:g.20311182T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.831T>A MANE Select	ENSP00000256906.4:p.Gly277=
ENST00000256906.4:c.831T>A	ENSP00000256906.4:p.Gly277=
ENST00000426880.2:c.567T>A	ENSP00000402526.2:p.Gly189=
NM_001143828.1:c.567T>A	NP_001137300.1:p.Gly189=
NM_001160166.1:c.*463T>A	NP_001153638.1:n.*463T>A
NM_021624.3:c.831T>A	NP_067637.2:p.Gly277=
XM_011526133.1:c.357+8269T>A	XP_011524435.1:n.357+8269T>A
NM_021624.4:c.831T>A MANE Select	NP_067637.2:p.Gly277=
NM_001143828.2:c.567T>A	NP_001137300.1:p.Gly189=
NM_001160166.2:c.*463T>A	NP_001153638.1:n.*463T>A