Canonical Allele Identifier: CA2001379823
Gene: HTR3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903417_113903418delinsTC , CM000673.2:g.113903417_113903418delinsTC GRCh38
NC_000011.9:g.113774139_113774140delinsTC , CM000673.1:g.113774139_113774140delinsTC GRCh37
NC_000011.8:g.113279349_113279350delinsTC NCBI36
NG_011483.1:g.3551_3552delinsTC

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4334_12+4335delinsTC XP_011541366.1:n.12+4334_12+4335delinsTC
XM_024448767.1:c.-243+4334_-243+4335delinsTC XP_024304535.1:n.-243+4334_-243+4335delinsTC