Canonical Allele Identifier: CA601784369
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs1159815566

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903428_113903432dup , CM000673.2:g.113903428_113903432dup GRCh38
NC_000011.9:g.113774150_113774154dup , CM000673.1:g.113774150_113774154dup GRCh37
NC_000011.8:g.113279360_113279364dup NCBI36
NG_011483.1:g.3562_3566dup

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4345_12+4349dup XP_011541366.1:n.12+4345_12+4349dup
XM_024448767.1:c.-243+4345_-243+4349dup XP_024304535.1:n.-243+4345_-243+4349dup