Canonical Allele Identifier: CA503523525

Gene: HRH4

Linked Data

• COSMIC: COSM4854108
• MyVariant Identifiers: chr18:g.22056884C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476920C>T , CM000680.2:g.24476920C>T	GRCh38
NC_000018.9:g.22056884C>T , CM000680.1:g.22056884C>T	GRCh37
NC_000018.8:g.20310882C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.531C>T MANE Select	ENSP00000256906.4:p.Ile177=
ENST00000256906.4:c.531C>T	ENSP00000256906.4:p.Ile177=
ENST00000426880.2:c.267C>T	ENSP00000402526.2:p.Ile89=
NM_001143828.1:c.267C>T	NP_001137300.1:p.Ile89=
NM_001160166.1:c.*163C>T	NP_001153638.1:n.*163C>T
NM_021624.3:c.531C>T	NP_067637.2:p.Ile177=
XM_011526133.1:c.357+7969C>T	XP_011524435.1:n.357+7969C>T
NM_021624.4:c.531C>T MANE Select	NP_067637.2:p.Ile177=
NM_001143828.2:c.267C>T	NP_001137300.1:p.Ile89=
NM_001160166.2:c.*163C>T	NP_001153638.1:n.*163C>T