Canonical Allele Identifier: CA2290574203
Gene: HRH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24469644A= , CM000680.2:g.24469644A= GRCh38
NC_000018.9:g.22049608A= , CM000680.1:g.22049608A= GRCh37
NC_000018.8:g.20303606A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.357+693A= MANE Select ENSP00000256906.4:n.357+693A=
ENST00000256906.4:c.357+693A= ENSP00000256906.4:n.357+693A=
ENST00000426880.2:c.194-7203A= ENSP00000402526.2:n.194-7203A=
NM_001143828.1:c.194-7203A= NP_001137300.1:n.194-7203A=
NM_001160166.1:c.194-7103A= NP_001153638.1:n.194-7103A=
NM_021624.3:c.357+693A= NP_067637.2:n.357+693A=
XM_011526133.1:c.357+693A= XP_011524435.1:n.357+693A=
XM_011526134.1:c.357+693A= XP_011524436.1:n.357+693A=
NM_021624.4:c.357+693A= MANE Select NP_067637.2:n.357+693A=
NM_001143828.2:c.194-7203A= NP_001137300.1:n.194-7203A=
NM_001160166.2:c.194-7103A= NP_001153638.1:n.194-7103A=