Canonical Allele Identifier: CA2001379838
Gene: HTR3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903428_113903440delinsCTTTTTTTTTTTT , CM000673.2:g.113903428_113903440delinsCTTTTTTTTTTTT GRCh38
NC_000011.9:g.113774150_113774162delinsCTTTTTTTTTTTT , CM000673.1:g.113774150_113774162delinsCTTTTTTTTTTTT GRCh37
NC_000011.8:g.113279360_113279372delinsCTTTTTTTTTTTT NCBI36
NG_011483.1:g.3562_3574delinsCTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4345_12+4357delinsCTTTTTTTTTTTT XP_011541366.1:n.12+4345_12+4357delinsCTTTTTTTTTTTT
XM_024448767.1:c.-243+4345_-243+4357delinsCTTTTTTTTTTTT XP_024304535.1:n.-243+4345_-243+4357delinsCTTTTTTTTTTTT