Canonical Allele Identifier: CA2290574197
Gene: HRH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24469631G= , CM000680.2:g.24469631G= GRCh38
NC_000018.9:g.22049595G= , CM000680.1:g.22049595G= GRCh37
NC_000018.8:g.20303593G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.357+680G= MANE Select ENSP00000256906.4:n.357+680G=
ENST00000256906.4:c.357+680G= ENSP00000256906.4:n.357+680G=
ENST00000426880.2:c.194-7216G= ENSP00000402526.2:n.194-7216G=
NM_001143828.1:c.194-7216G= NP_001137300.1:n.194-7216G=
NM_001160166.1:c.194-7116G= NP_001153638.1:n.194-7116G=
NM_021624.3:c.357+680G= NP_067637.2:n.357+680G=
XM_011526133.1:c.357+680G= XP_011524435.1:n.357+680G=
XM_011526134.1:c.357+680G= XP_011524436.1:n.357+680G=
NM_021624.4:c.357+680G= MANE Select NP_067637.2:n.357+680G=
NM_001143828.2:c.194-7216G= NP_001137300.1:n.194-7216G=
NM_001160166.2:c.194-7116G= NP_001153638.1:n.194-7116G=