Canonical Allele Identifier: CA402083220
Gene: HRH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.22057018A>G (hg19) chr18:g.24477054A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24477054A>G , CM000680.2:g.24477054A>G GRCh38
NC_000018.9:g.22057018A>G , CM000680.1:g.22057018A>G GRCh37
NC_000018.8:g.20311016A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.665A>G MANE Select ENSP00000256906.4:p.Asn222Ser
ENST00000256906.4:c.665A>G ENSP00000256906.4:p.Asn222Ser
ENST00000426880.2:c.401A>G ENSP00000402526.2:p.Asn134Ser
NM_001143828.1:c.401A>G NP_001137300.1:p.Asn134Ser
NM_001160166.1:c.*297A>G NP_001153638.1:n.*297A>G
NM_021624.3:c.665A>G NP_067637.2:p.Asn222Ser
XM_011526133.1:c.357+8103A>G XP_011524435.1:n.357+8103A>G
NM_021624.4:c.665A>G MANE Select NP_067637.2:p.Asn222Ser
NM_001143828.2:c.401A>G NP_001137300.1:p.Asn134Ser
NM_001160166.2:c.*297A>G NP_001153638.1:n.*297A>G
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