Canonical Allele Identifier: CA503523701

Gene: HRH4

Linked Data

• MyVariant Identifiers: chr18:g.22057109A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24477145A>G , CM000680.2:g.24477145A>G	GRCh38
NC_000018.9:g.22057109A>G , CM000680.1:g.22057109A>G	GRCh37
NC_000018.8:g.20311107A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.756A>G MANE Select	ENSP00000256906.4:p.Arg252=
ENST00000256906.4:c.756A>G	ENSP00000256906.4:p.Arg252=
ENST00000426880.2:c.492A>G	ENSP00000402526.2:p.Arg164=
NM_001143828.1:c.492A>G	NP_001137300.1:p.Arg164=
NM_001160166.1:c.*388A>G	NP_001153638.1:n.*388A>G
NM_021624.3:c.756A>G	NP_067637.2:p.Arg252=
XM_011526133.1:c.357+8194A>G	XP_011524435.1:n.357+8194A>G
NM_021624.4:c.756A>G MANE Select	NP_067637.2:p.Arg252=
NM_001143828.2:c.492A>G	NP_001137300.1:p.Arg164=
NM_001160166.2:c.*388A>G	NP_001153638.1:n.*388A>G