Canonical Allele Identifier: CA2641326626
Gene: HRH4 HGNC NCBI

Linked Data

gnomAD v4: 18-24476634-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476634T>G , CM000680.2:g.24476634T>G GRCh38
NC_000018.9:g.22056598T>G , CM000680.1:g.22056598T>G GRCh37
NC_000018.8:g.20310596T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.358-113T>G MANE Select ENSP00000256906.4:n.358-113T>G
ENST00000256906.4:c.358-113T>G ENSP00000256906.4:n.358-113T>G
ENST00000426880.2:c.194-213T>G ENSP00000402526.2:n.194-213T>G
NM_001143828.1:c.194-213T>G NP_001137300.1:n.194-213T>G
NM_001160166.1:c.194-113T>G NP_001153638.1:n.194-113T>G
NM_021624.3:c.358-113T>G NP_067637.2:n.358-113T>G
XM_011526133.1:c.357+7683T>G XP_011524435.1:n.357+7683T>G
NM_021624.4:c.358-113T>G MANE Select NP_067637.2:n.358-113T>G
NM_001143828.2:c.194-213T>G NP_001137300.1:n.194-213T>G
NM_001160166.2:c.194-113T>G NP_001153638.1:n.194-113T>G
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