Canonical Allele Identifier: CA402082884
Gene: HRH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.22056867T>C (hg19) chr18:g.24476903T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476903T>C , CM000680.2:g.24476903T>C GRCh38
NC_000018.9:g.22056867T>C , CM000680.1:g.22056867T>C GRCh37
NC_000018.8:g.20310865T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.514T>C MANE Select ENSP00000256906.4:p.Trp172Arg
ENST00000256906.4:c.514T>C ENSP00000256906.4:p.Trp172Arg
ENST00000426880.2:c.250T>C ENSP00000402526.2:p.Trp84Arg
NM_001143828.1:c.250T>C NP_001137300.1:p.Trp84Arg
NM_001160166.1:c.*146T>C NP_001153638.1:n.*146T>C
NM_021624.3:c.514T>C NP_067637.2:p.Trp172Arg
XM_011526133.1:c.357+7952T>C XP_011524435.1:n.357+7952T>C
NM_021624.4:c.514T>C MANE Select NP_067637.2:p.Trp172Arg
NM_001143828.2:c.250T>C NP_001137300.1:p.Trp84Arg
NM_001160166.2:c.*146T>C NP_001153638.1:n.*146T>C
Search 100 bp 5'
Search 100 bp 3'