Canonical Allele Identifier: CA2290577508
Gene: HRH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24476707T= , CM000680.2:g.24476707T= GRCh38
NC_000018.9:g.22056671T= , CM000680.1:g.22056671T= GRCh37
NC_000018.8:g.20310669T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000256906.5:c.358-40T= MANE Select ENSP00000256906.4:n.358-40T=
ENST00000256906.4:c.358-40T= ENSP00000256906.4:n.358-40T=
ENST00000426880.2:c.194-140T= ENSP00000402526.2:n.194-140T=
NM_001143828.1:c.194-140T= NP_001137300.1:n.194-140T=
NM_001160166.1:c.194-40T= NP_001153638.1:n.194-40T=
NM_021624.3:c.358-40T= NP_067637.2:n.358-40T=
XM_011526133.1:c.357+7756T= XP_011524435.1:n.357+7756T=
NM_021624.4:c.358-40T= MANE Select NP_067637.2:n.358-40T=
NM_001143828.2:c.194-140T= NP_001137300.1:n.194-140T=
NM_001160166.2:c.194-40T= NP_001153638.1:n.194-40T=