Canonical Allele Identifier: CA2576475256
Gene: HRH4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24460639A>T , CM000680.2:g.24460639A>T GRCh38
NC_000018.9:g.22040603A>T , CM000680.1:g.22040603A>T GRCh37
NC_000018.8:g.20294601A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.-90A>T MANE Select ENSP00000256906.4:n.-90A>T
ENST00000256906.4:c.-90A>T ENSP00000256906.4:n.-90A>T
NM_001143828.1:c.-90A>T NP_001137300.1:n.-90A>T
NM_001160166.1:c.-90A>T NP_001153638.1:n.-90A>T
NM_021624.3:c.-90A>T NP_067637.2:n.-90A>T
XM_011526133.1:c.-90A>T XP_011524435.1:n.-90A>T
XM_011526134.1:c.-90A>T XP_011524436.1:n.-90A>T
NM_021624.4:c.-90A>T MANE Select NP_067637.2:n.-90A>T
NM_001143828.2:c.-90A>T NP_001137300.1:n.-90A>T
NM_001160166.2:c.-90A>T NP_001153638.1:n.-90A>T