Canonical Allele Identifier: CA2001379853
Gene: HTR3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903446_113903448delinsTTG , CM000673.2:g.113903446_113903448delinsTTG GRCh38
NC_000011.9:g.113774168_113774170delinsTTG , CM000673.1:g.113774168_113774170delinsTTG GRCh37
NC_000011.8:g.113279378_113279380delinsTTG NCBI36
NG_011483.1:g.3580_3582delinsTTG

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4363_12+4365delinsTTG XP_011541366.1:n.12+4363_12+4365delinsTTG
XM_024448767.1:c.-243+4363_-243+4365delinsTTG XP_024304535.1:n.-243+4363_-243+4365delinsTTG