Canonical Allele Identifier: CA402082826

Gene: HRH4

Linked Data

• gnomAD v4: 18-24476877-A-T
• MyVariant Identifiers: chr18:g.22056841A>T (hg19) ; chr18:g.24476877A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476877A>T , CM000680.2:g.24476877A>T	GRCh38
NC_000018.9:g.22056841A>T , CM000680.1:g.22056841A>T	GRCh37
NC_000018.8:g.20310839A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256906.5:c.488A>T MANE Select	ENSP00000256906.4:p.Glu163Val
ENST00000256906.4:c.488A>T	ENSP00000256906.4:p.Glu163Val
ENST00000426880.2:c.224A>T	ENSP00000402526.2:p.Glu75Val
NM_001143828.1:c.224A>T	NP_001137300.1:p.Glu75Val
NM_001160166.1:c.*120A>T	NP_001153638.1:n.*120A>T
NM_021624.3:c.488A>T	NP_067637.2:p.Glu163Val
XM_011526133.1:c.357+7926A>T	XP_011524435.1:n.357+7926A>T
NM_021624.4:c.488A>T MANE Select	NP_067637.2:p.Glu163Val
NM_001143828.2:c.224A>T	NP_001137300.1:p.Glu75Val
NM_001160166.2:c.*120A>T	NP_001153638.1:n.*120A>T