Canonical Allele Identifier: CA402082778
Gene: HRH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.22056822T>A (hg19) chr18:g.24476858T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476858T>A , CM000680.2:g.24476858T>A GRCh38
NC_000018.9:g.22056822T>A , CM000680.1:g.22056822T>A GRCh37
NC_000018.8:g.20310820T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.469T>A MANE Select ENSP00000256906.4:p.Trp157Arg
ENST00000256906.4:c.469T>A ENSP00000256906.4:p.Trp157Arg
ENST00000426880.2:c.205T>A ENSP00000402526.2:p.Trp69Arg
NM_001143828.1:c.205T>A NP_001137300.1:p.Trp69Arg
NM_001160166.1:c.*101T>A NP_001153638.1:n.*101T>A
NM_021624.3:c.469T>A NP_067637.2:p.Trp157Arg
XM_011526133.1:c.357+7907T>A XP_011524435.1:n.357+7907T>A
NM_021624.4:c.469T>A MANE Select NP_067637.2:p.Trp157Arg
NM_001143828.2:c.205T>A NP_001137300.1:p.Trp69Arg
NM_001160166.2:c.*101T>A NP_001153638.1:n.*101T>A
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