Canonical Allele Identifier: CA8919887
Gene: HRH4 HGNC NCBI

Linked Data

dbSNP Id: rs773223791

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24477233T>C , CM000680.2:g.24477233T>C GRCh38
NC_000018.9:g.22057197T>C , CM000680.1:g.22057197T>C GRCh37
NC_000018.8:g.20311195T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.844T>C MANE Select ENSP00000256906.4:p.Ser282Pro
ENST00000256906.4:c.844T>C ENSP00000256906.4:p.Ser282Pro
ENST00000426880.2:c.580T>C ENSP00000402526.2:p.Ser194Pro
NM_001143828.1:c.580T>C NP_001137300.1:p.Ser194Pro
NM_001160166.1:c.*476T>C NP_001153638.1:n.*476T>C
NM_021624.3:c.844T>C NP_067637.2:p.Ser282Pro
XM_011526133.1:c.357+8282T>C XP_011524435.1:n.357+8282T>C
NM_021624.4:c.844T>C MANE Select NP_067637.2:p.Ser282Pro
NM_001143828.2:c.580T>C NP_001137300.1:p.Ser194Pro
NM_001160166.2:c.*476T>C NP_001153638.1:n.*476T>C