Canonical Allele Identifier: CA402083165
Gene: HRH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.22056990C>G (hg19) chr18:g.24477026C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24477026C>G , CM000680.2:g.24477026C>G GRCh38
NC_000018.9:g.22056990C>G , CM000680.1:g.22056990C>G GRCh37
NC_000018.8:g.20310988C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000256906.5:c.637C>G MANE Select ENSP00000256906.4:p.His213Asp
ENST00000256906.4:c.637C>G ENSP00000256906.4:p.His213Asp
ENST00000426880.2:c.373C>G ENSP00000402526.2:p.His125Asp
NM_001143828.1:c.373C>G NP_001137300.1:p.His125Asp
NM_001160166.1:c.*269C>G NP_001153638.1:n.*269C>G
NM_021624.3:c.637C>G NP_067637.2:p.His213Asp
XM_011526133.1:c.357+8075C>G XP_011524435.1:n.357+8075C>G
NM_021624.4:c.637C>G MANE Select NP_067637.2:p.His213Asp
NM_001143828.2:c.373C>G NP_001137300.1:p.His125Asp
NM_001160166.2:c.*269C>G NP_001153638.1:n.*269C>G
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