Canonical Allele Identifier: CA2290570369
Gene: HRH4 HGNC NCBI

Linked Data

dbSNP Id: rs1909606585

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24460628T>G , CM000680.2:g.24460628T>G GRCh38
NC_000018.9:g.22040592T>G , CM000680.1:g.22040592T>G GRCh37
NC_000018.8:g.20294590T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011526133.1:c.-101T>G XP_011524435.1:n.-101T>G
XM_011526134.1:c.-101T>G XP_011524436.1:n.-101T>G