Canonical Allele Identifier: CA2793690762
Gene: HTR3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903432_113903433insCTTT , CM000673.2:g.113903432_113903433insCTTT GRCh38
NC_000011.9:g.113774154_113774155insCTTT , CM000673.1:g.113774154_113774155insCTTT GRCh37
NC_000011.8:g.113279364_113279365insCTTT NCBI36
NG_011483.1:g.3566_3567insCTTT

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4349_12+4350insCTTT XP_011541366.1:n.12+4349_12+4350insCTTT
XM_024448767.1:c.-243+4349_-243+4350insCTTT XP_024304535.1:n.-243+4349_-243+4350insCTTT