Canonical Allele Identifier: CA402083052

Gene: HRH4

Linked Data

• MyVariant Identifiers: chr18:g.22056942A>G (hg19) ; chr18:g.24476978A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476978A>G , CM000680.2:g.24476978A>G	GRCh38
NC_000018.9:g.22056942A>G , CM000680.1:g.22056942A>G	GRCh37
NC_000018.8:g.20310940A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.589A>G MANE Select	ENSP00000256906.4:p.Ile197Val
ENST00000256906.4:c.589A>G	ENSP00000256906.4:p.Ile197Val
ENST00000426880.2:c.325A>G	ENSP00000402526.2:p.Ile109Val
NM_001143828.1:c.325A>G	NP_001137300.1:p.Ile109Val
NM_001160166.1:c.*221A>G	NP_001153638.1:n.*221A>G
NM_021624.3:c.589A>G	NP_067637.2:p.Ile197Val
XM_011526133.1:c.357+8027A>G	XP_011524435.1:n.357+8027A>G
NM_021624.4:c.589A>G MANE Select	NP_067637.2:p.Ile197Val
NM_001143828.2:c.325A>G	NP_001137300.1:p.Ile109Val
NM_001160166.2:c.*221A>G	NP_001153638.1:n.*221A>G