Canonical Allele Identifier: CA2641326605
Gene: HRH4 HGNC NCBI

Linked Data

gnomAD v4: 18-24476618-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476618C>A , CM000680.2:g.24476618C>A GRCh38
NC_000018.9:g.22056582C>A , CM000680.1:g.22056582C>A GRCh37
NC_000018.8:g.20310580C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000256906.5:c.358-129C>A MANE Select ENSP00000256906.4:n.358-129C>A
ENST00000256906.4:c.358-129C>A ENSP00000256906.4:n.358-129C>A
ENST00000426880.2:c.194-229C>A ENSP00000402526.2:n.194-229C>A
NM_001143828.1:c.194-229C>A NP_001137300.1:n.194-229C>A
NM_001160166.1:c.194-129C>A NP_001153638.1:n.194-129C>A
NM_021624.3:c.358-129C>A NP_067637.2:n.358-129C>A
XM_011526133.1:c.357+7667C>A XP_011524435.1:n.357+7667C>A
NM_021624.4:c.358-129C>A MANE Select NP_067637.2:n.358-129C>A
NM_001143828.2:c.194-229C>A NP_001137300.1:n.194-229C>A
NM_001160166.2:c.194-129C>A NP_001153638.1:n.194-129C>A
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