Canonical Allele Identifier: CA2001379855
Gene: HTR3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903447_113903448delinsTG , CM000673.2:g.113903447_113903448delinsTG GRCh38
NC_000011.9:g.113774169_113774170delinsTG , CM000673.1:g.113774169_113774170delinsTG GRCh37
NC_000011.8:g.113279379_113279380delinsTG NCBI36
NG_011483.1:g.3581_3582delinsTG

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4364_12+4365delinsTG XP_011541366.1:n.12+4364_12+4365delinsTG
XM_024448767.1:c.-243+4364_-243+4365delinsTG XP_024304535.1:n.-243+4364_-243+4365delinsTG