Canonical Allele Identifier: CA2290570377
Gene: HRH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24460637A= , CM000680.2:g.24460637A= GRCh38
NC_000018.9:g.22040601A= , CM000680.1:g.22040601A= GRCh37
NC_000018.8:g.20294599A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.-92A= MANE Select ENSP00000256906.4:n.-92A=
ENST00000256906.4:c.-92A= ENSP00000256906.4:n.-92A=
NM_001143828.1:c.-92A= NP_001137300.1:n.-92A=
NM_001160166.1:c.-92A= NP_001153638.1:n.-92A=
NM_021624.3:c.-92A= NP_067637.2:n.-92A=
XM_011526133.1:c.-92A= XP_011524435.1:n.-92A=
XM_011526134.1:c.-92A= XP_011524436.1:n.-92A=
NM_021624.4:c.-92A= MANE Select NP_067637.2:n.-92A=
NM_001143828.2:c.-92A= NP_001137300.1:n.-92A=
NM_001160166.2:c.-92A= NP_001153638.1:n.-92A=