Canonical Allele Identifier: CA402083379
Gene: HRH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.22057095T>A (hg19) chr18:g.24477131T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24477131T>A , CM000680.2:g.24477131T>A GRCh38
NC_000018.9:g.22057095T>A , CM000680.1:g.22057095T>A GRCh37
NC_000018.8:g.20311093T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.742T>A MANE Select ENSP00000256906.4:p.Phe248Ile
ENST00000256906.4:c.742T>A ENSP00000256906.4:p.Phe248Ile
ENST00000426880.2:c.478T>A ENSP00000402526.2:p.Phe160Ile
NM_001143828.1:c.478T>A NP_001137300.1:p.Phe160Ile
NM_001160166.1:c.*374T>A NP_001153638.1:n.*374T>A
NM_021624.3:c.742T>A NP_067637.2:p.Phe248Ile
XM_011526133.1:c.357+8180T>A XP_011524435.1:n.357+8180T>A
NM_021624.4:c.742T>A MANE Select NP_067637.2:p.Phe248Ile
NM_001143828.2:c.478T>A NP_001137300.1:p.Phe160Ile
NM_001160166.2:c.*374T>A NP_001153638.1:n.*374T>A
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