Canonical Allele Identifier: CA2290570371
Gene: HRH4 HGNC NCBI

Linked Data

dbSNP Id: rs1909606645

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24460630del , CM000680.2:g.24460630del GRCh38
NC_000018.9:g.22040594del , CM000680.1:g.22040594del GRCh37
NC_000018.8:g.20294592del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.4:c.-99del ENSP00000256906.4:n.-99del
NM_001143828.1:c.-99del NP_001137300.1:n.-99del
NM_001160166.1:c.-99del NP_001153638.1:n.-99del
NM_021624.3:c.-99del NP_067637.2:n.-99del
XM_011526133.1:c.-99del XP_011524435.1:n.-99del
XM_011526134.1:c.-99del XP_011524436.1:n.-99del