Canonical Allele Identifier: CA503523514

Gene: HRH4

Linked Data

• COSMIC: COSM3959083
• MyVariant Identifiers: chr18:g.22056875C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476911C>A , CM000680.2:g.24476911C>A	GRCh38
NC_000018.9:g.22056875C>A , CM000680.1:g.22056875C>A	GRCh37
NC_000018.8:g.20310873C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.522C>A MANE Select	ENSP00000256906.4:p.Ile174=
ENST00000256906.4:c.522C>A	ENSP00000256906.4:p.Ile174=
ENST00000426880.2:c.258C>A	ENSP00000402526.2:p.Ile86=
NM_001143828.1:c.258C>A	NP_001137300.1:p.Ile86=
NM_001160166.1:c.*154C>A	NP_001153638.1:n.*154C>A
NM_021624.3:c.522C>A	NP_067637.2:p.Ile174=
XM_011526133.1:c.357+7960C>A	XP_011524435.1:n.357+7960C>A
NM_021624.4:c.522C>A MANE Select	NP_067637.2:p.Ile174=
NM_001143828.2:c.258C>A	NP_001137300.1:p.Ile86=
NM_001160166.2:c.*154C>A	NP_001153638.1:n.*154C>A