Canonical Allele Identifier: CA402083626
Gene: HRH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.22057206G>A (hg19) chr18:g.24477242G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24477242G>A , CM000680.2:g.24477242G>A GRCh38
NC_000018.9:g.22057206G>A , CM000680.1:g.22057206G>A GRCh37
NC_000018.8:g.20311204G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.853G>A MANE Select ENSP00000256906.4:p.Val285Ile
ENST00000256906.4:c.853G>A ENSP00000256906.4:p.Val285Ile
ENST00000426880.2:c.589G>A ENSP00000402526.2:p.Val197Ile
NM_001143828.1:c.589G>A NP_001137300.1:p.Val197Ile
NM_001160166.1:c.*485G>A NP_001153638.1:n.*485G>A
NM_021624.3:c.853G>A NP_067637.2:p.Val285Ile
XM_011526133.1:c.357+8291G>A XP_011524435.1:n.357+8291G>A
NM_021624.4:c.853G>A MANE Select NP_067637.2:p.Val285Ile
NM_001143828.2:c.589G>A NP_001137300.1:p.Val197Ile
NM_001160166.2:c.*485G>A NP_001153638.1:n.*485G>A
Search 100 bp 5'
Search 100 bp 3'