Canonical Allele Identifier: CA503523799
Gene: HRH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.22057184T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24477220T>C , CM000680.2:g.24477220T>C GRCh38
NC_000018.9:g.22057184T>C , CM000680.1:g.22057184T>C GRCh37
NC_000018.8:g.20311182T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.831T>C MANE Select ENSP00000256906.4:p.Gly277=
ENST00000256906.4:c.831T>C ENSP00000256906.4:p.Gly277=
ENST00000426880.2:c.567T>C ENSP00000402526.2:p.Gly189=
NM_001143828.1:c.567T>C NP_001137300.1:p.Gly189=
NM_001160166.1:c.*463T>C NP_001153638.1:n.*463T>C
NM_021624.3:c.831T>C NP_067637.2:p.Gly277=
XM_011526133.1:c.357+8269T>C XP_011524435.1:n.357+8269T>C
NM_021624.4:c.831T>C MANE Select NP_067637.2:p.Gly277=
NM_001143828.2:c.567T>C NP_001137300.1:p.Gly189=
NM_001160166.2:c.*463T>C NP_001153638.1:n.*463T>C
Search 100 bp 5'
Search 100 bp 3'