Canonical Allele Identifier: CA402082908
Gene: HRH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.22056876C>A (hg19) chr18:g.24476912C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476912C>A , CM000680.2:g.24476912C>A GRCh38
NC_000018.9:g.22056876C>A , CM000680.1:g.22056876C>A GRCh37
NC_000018.8:g.20310874C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.523C>A MANE Select ENSP00000256906.4:p.Leu175Ile
ENST00000256906.4:c.523C>A ENSP00000256906.4:p.Leu175Ile
ENST00000426880.2:c.259C>A ENSP00000402526.2:p.Leu87Ile
NM_001143828.1:c.259C>A NP_001137300.1:p.Leu87Ile
NM_001160166.1:c.*155C>A NP_001153638.1:n.*155C>A
NM_021624.3:c.523C>A NP_067637.2:p.Leu175Ile
XM_011526133.1:c.357+7961C>A XP_011524435.1:n.357+7961C>A
NM_021624.4:c.523C>A MANE Select NP_067637.2:p.Leu175Ile
NM_001143828.2:c.259C>A NP_001137300.1:p.Leu87Ile
NM_001160166.2:c.*155C>A NP_001153638.1:n.*155C>A
Search 100 bp 5'
Search 100 bp 3'