Canonical Allele Identifier: CA503523835

Gene: HRH4

Linked Data

• MyVariant Identifiers: chr18:g.22057211T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24477247T>G , CM000680.2:g.24477247T>G	GRCh38
NC_000018.9:g.22057211T>G , CM000680.1:g.22057211T>G	GRCh37
NC_000018.8:g.20311209T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.858T>G MANE Select	ENSP00000256906.4:p.Ala286=
ENST00000256906.4:c.858T>G	ENSP00000256906.4:p.Ala286=
ENST00000426880.2:c.594T>G	ENSP00000402526.2:p.Ala198=
NM_001143828.1:c.594T>G	NP_001137300.1:p.Ala198=
NM_001160166.1:c.*490T>G	NP_001153638.1:n.*490T>G
NM_021624.3:c.858T>G	NP_067637.2:p.Ala286=
XM_011526133.1:c.357+8296T>G	XP_011524435.1:n.357+8296T>G
NM_021624.4:c.858T>G MANE Select	NP_067637.2:p.Ala286=
NM_001143828.2:c.594T>G	NP_001137300.1:p.Ala198=
NM_001160166.2:c.*490T>G	NP_001153638.1:n.*490T>G