Canonical Allele Identifier: CA402083639
Gene: HRH4 HGNC NCBI

Linked Data

dbSNP Id: rs1910167242

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24477248C>T , CM000680.2:g.24477248C>T GRCh38
NC_000018.9:g.22057212C>T , CM000680.1:g.22057212C>T GRCh37
NC_000018.8:g.20311210C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.859C>T MANE Select ENSP00000256906.4:p.Leu287Phe
ENST00000256906.4:c.859C>T ENSP00000256906.4:p.Leu287Phe
ENST00000426880.2:c.595C>T ENSP00000402526.2:p.Leu199Phe
NM_001143828.1:c.595C>T NP_001137300.1:p.Leu199Phe
NM_001160166.1:c.*491C>T NP_001153638.1:n.*491C>T
NM_021624.3:c.859C>T NP_067637.2:p.Leu287Phe
XM_011526133.1:c.357+8297C>T XP_011524435.1:n.357+8297C>T
NM_021624.4:c.859C>T MANE Select NP_067637.2:p.Leu287Phe
NM_001143828.2:c.595C>T NP_001137300.1:p.Leu199Phe
NM_001160166.2:c.*491C>T NP_001153638.1:n.*491C>T