Canonical Allele Identifier: CA2290574165
Gene: HRH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24469567A= , CM000680.2:g.24469567A= GRCh38
NC_000018.9:g.22049531A= , CM000680.1:g.22049531A= GRCh37
NC_000018.8:g.20303529A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.357+616A= MANE Select ENSP00000256906.4:n.357+616A=
ENST00000256906.4:c.357+616A= ENSP00000256906.4:n.357+616A=
ENST00000426880.2:c.194-7280A= ENSP00000402526.2:n.194-7280A=
NM_001143828.1:c.194-7280A= NP_001137300.1:n.194-7280A=
NM_001160166.1:c.194-7180A= NP_001153638.1:n.194-7180A=
NM_021624.3:c.357+616A= NP_067637.2:n.357+616A=
XM_011526133.1:c.357+616A= XP_011524435.1:n.357+616A=
XM_011526134.1:c.357+616A= XP_011524436.1:n.357+616A=
NM_021624.4:c.357+616A= MANE Select NP_067637.2:n.357+616A=
NM_001143828.2:c.194-7280A= NP_001137300.1:n.194-7280A=
NM_001160166.2:c.194-7180A= NP_001153638.1:n.194-7180A=