Canonical Allele Identifier: CA402083498
Gene: HRH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.22057147C>A (hg19) chr18:g.24477183C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24477183C>A , CM000680.2:g.24477183C>A GRCh38
NC_000018.9:g.22057147C>A , CM000680.1:g.22057147C>A GRCh37
NC_000018.8:g.20311145C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.794C>A MANE Select ENSP00000256906.4:p.Thr265Asn
ENST00000256906.4:c.794C>A ENSP00000256906.4:p.Thr265Asn
ENST00000426880.2:c.530C>A ENSP00000402526.2:p.Thr177Asn
NM_001143828.1:c.530C>A NP_001137300.1:p.Thr177Asn
NM_001160166.1:c.*426C>A NP_001153638.1:n.*426C>A
NM_021624.3:c.794C>A NP_067637.2:p.Thr265Asn
XM_011526133.1:c.357+8232C>A XP_011524435.1:n.357+8232C>A
NM_021624.4:c.794C>A MANE Select NP_067637.2:p.Thr265Asn
NM_001143828.2:c.530C>A NP_001137300.1:p.Thr177Asn
NM_001160166.2:c.*426C>A NP_001153638.1:n.*426C>A
Search 100 bp 5'
Search 100 bp 3'