Canonical Allele Identifier: CA402082960

Gene: HRH4

Linked Data

• MyVariant Identifiers: chr18:g.22056901T>A (hg19) ; chr18:g.24476937T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476937T>A , CM000680.2:g.24476937T>A	GRCh38
NC_000018.9:g.22056901T>A , CM000680.1:g.22056901T>A	GRCh37
NC_000018.8:g.20310899T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.548T>A MANE Select	ENSP00000256906.4:p.Phe183Tyr
ENST00000256906.4:c.548T>A	ENSP00000256906.4:p.Phe183Tyr
ENST00000426880.2:c.284T>A	ENSP00000402526.2:p.Phe95Tyr
NM_001143828.1:c.284T>A	NP_001137300.1:p.Phe95Tyr
NM_001160166.1:c.*180T>A	NP_001153638.1:n.*180T>A
NM_021624.3:c.548T>A	NP_067637.2:p.Phe183Tyr
XM_011526133.1:c.357+7986T>A	XP_011524435.1:n.357+7986T>A
NM_021624.4:c.548T>A MANE Select	NP_067637.2:p.Phe183Tyr
NM_001143828.2:c.284T>A	NP_001137300.1:p.Phe95Tyr
NM_001160166.2:c.*180T>A	NP_001153638.1:n.*180T>A