Canonical Allele Identifier: CA432305808

Gene: HRH1

Linked Data

• COSMIC: COSM3845843
• MyVariant Identifiers: chr3:g.11301539C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.11259853C>G , CM000665.2:g.11259853C>G	GRCh38
NC_000003.11:g.11301539C>G , CM000665.1:g.11301539C>G	GRCh37
NC_000003.10:g.11276539C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000431010.3:c.816C>G MANE Select	ENSP00000397028.2:p.Val272=
ENST00000397056.1:c.816C>G	ENSP00000380247.1:p.Val272=
ENST00000431010.2:c.816C>G	ENSP00000397028.2:p.Val272=
ENST00000438284.2:c.816C>G	ENSP00000406705.2:p.Val272=
NM_000861.3:c.816C>G	NP_000852.1:p.Val272=
NM_001098211.1:c.816C>G	NP_001091681.1:p.Val272=
NM_001098212.1:c.816C>G	NP_001091682.1:p.Val272=
NM_001098213.1:c.816C>G	NP_001091683.1:p.Val272=
XM_011533652.1:c.816C>G	XP_011531954.1:p.Val272=
XM_011533653.1:c.816C>G	XP_011531955.1:p.Val272=
XM_011533654.1:c.816C>G	XP_011531956.1:p.Val272=
XM_011533655.1:c.816C>G	XP_011531957.1:p.Val272=
XM_011533653.2:c.816C>G	XP_011531955.1:p.Val272=
XM_017006283.1:c.816C>G	XP_016861772.1:p.Val272=
XM_017006284.1:c.816C>G	XP_016861773.1:p.Val272=
NM_001098211.2:c.816C>G	NP_001091681.1:p.Val272=
NM_001098212.2:c.816C>G MANE Select	NP_001091682.1:p.Val272=
NM_001098213.2:c.816C>G	NP_001091683.1:p.Val272=