Canonical Allele Identifier: CA8919825
Gene: HRH4 HGNC NCBI

Linked Data

dbSNP Id: rs753915955
ExAC: 18:22056866 A / G
gnomAD v2: 18-22056866-A-G
gnomAD v3: 18-24476902-A-G
gnomAD v4: 18-24476902-A-G
MyVariant Identifiers: chr18:g.22056866A>G (hg19) chr18:g.24476902A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476902A>G , CM000680.2:g.24476902A>G GRCh38
NC_000018.9:g.22056866A>G , CM000680.1:g.22056866A>G GRCh37
NC_000018.8:g.20310864A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.513A>G MANE Select ENSP00000256906.4:p.Glu171=
ENST00000256906.4:c.513A>G ENSP00000256906.4:p.Glu171=
ENST00000426880.2:c.249A>G ENSP00000402526.2:p.Glu83=
NM_001143828.1:c.249A>G NP_001137300.1:p.Glu83=
NM_001160166.1:c.*145A>G NP_001153638.1:n.*145A>G
NM_021624.3:c.513A>G NP_067637.2:p.Glu171=
XM_011526133.1:c.357+7951A>G XP_011524435.1:n.357+7951A>G
NM_021624.4:c.513A>G MANE Select NP_067637.2:p.Glu171=
NM_001143828.2:c.249A>G NP_001137300.1:p.Glu83=
NM_001160166.2:c.*145A>G NP_001153638.1:n.*145A>G
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