Canonical Allele Identifier: CA8919790
Gene: HRH4 HGNC NCBI

Linked Data

dbSNP Id: rs373456077
ExAC: 18:22056677 T / C
gnomAD v2: 18-22056677-T-C
gnomAD v3: 18-24476713-T-C
gnomAD v4: 18-24476713-T-C
MyVariant Identifiers: chr18:g.22056677T>C (hg19) chr18:g.24476713T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476713T>C , CM000680.2:g.24476713T>C GRCh38
NC_000018.9:g.22056677T>C , CM000680.1:g.22056677T>C GRCh37
NC_000018.8:g.20310675T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000256906.5:c.358-34T>C MANE Select ENSP00000256906.4:n.358-34T>C
ENST00000256906.4:c.358-34T>C ENSP00000256906.4:n.358-34T>C
ENST00000426880.2:c.194-134T>C ENSP00000402526.2:n.194-134T>C
NM_001143828.1:c.194-134T>C NP_001137300.1:n.194-134T>C
NM_001160166.1:c.194-34T>C NP_001153638.1:n.194-34T>C
NM_021624.3:c.358-34T>C NP_067637.2:n.358-34T>C
XM_011526133.1:c.357+7762T>C XP_011524435.1:n.357+7762T>C
NM_021624.4:c.358-34T>C MANE Select NP_067637.2:n.358-34T>C
NM_001143828.2:c.194-134T>C NP_001137300.1:n.194-134T>C
NM_001160166.2:c.194-34T>C NP_001153638.1:n.194-34T>C
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