Canonical Allele Identifier: CA402083477
Gene: HRH4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.22057137T>C (hg19) chr18:g.24477173T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24477173T>C , CM000680.2:g.24477173T>C GRCh38
NC_000018.9:g.22057137T>C , CM000680.1:g.22057137T>C GRCh37
NC_000018.8:g.20311135T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.784T>C MANE Select ENSP00000256906.4:p.Ser262Pro
ENST00000256906.4:c.784T>C ENSP00000256906.4:p.Ser262Pro
ENST00000426880.2:c.520T>C ENSP00000402526.2:p.Ser174Pro
NM_001143828.1:c.520T>C NP_001137300.1:p.Ser174Pro
NM_001160166.1:c.*416T>C NP_001153638.1:n.*416T>C
NM_021624.3:c.784T>C NP_067637.2:p.Ser262Pro
XM_011526133.1:c.357+8222T>C XP_011524435.1:n.357+8222T>C
NM_021624.4:c.784T>C MANE Select NP_067637.2:p.Ser262Pro
NM_001143828.2:c.520T>C NP_001137300.1:p.Ser174Pro
NM_001160166.2:c.*416T>C NP_001153638.1:n.*416T>C
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