Canonical Allele Identifier: CA2641326606
Gene: HRH4 HGNC NCBI

Linked Data

gnomAD v4: 18-24476619-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476619A>T , CM000680.2:g.24476619A>T GRCh38
NC_000018.9:g.22056583A>T , CM000680.1:g.22056583A>T GRCh37
NC_000018.8:g.20310581A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.358-128A>T MANE Select ENSP00000256906.4:n.358-128A>T
ENST00000256906.4:c.358-128A>T ENSP00000256906.4:n.358-128A>T
ENST00000426880.2:c.194-228A>T ENSP00000402526.2:n.194-228A>T
NM_001143828.1:c.194-228A>T NP_001137300.1:n.194-228A>T
NM_001160166.1:c.194-128A>T NP_001153638.1:n.194-128A>T
NM_021624.3:c.358-128A>T NP_067637.2:n.358-128A>T
XM_011526133.1:c.357+7668A>T XP_011524435.1:n.357+7668A>T
NM_021624.4:c.358-128A>T MANE Select NP_067637.2:n.358-128A>T
NM_001143828.2:c.194-228A>T NP_001137300.1:n.194-228A>T
NM_001160166.2:c.194-128A>T NP_001153638.1:n.194-128A>T
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