Canonical Allele Identifier: CA942403976
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs57289369

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903437_113903447dup , CM000673.2:g.113903437_113903447dup GRCh38
NC_000011.9:g.113774159_113774169dup , CM000673.1:g.113774159_113774169dup GRCh37
NC_000011.8:g.113279369_113279379dup NCBI36
NG_011483.1:g.3571_3581dup

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4354_12+4364dup XP_011541366.1:n.12+4354_12+4364dup
XM_024448767.1:c.-243+4354_-243+4364dup XP_024304535.1:n.-243+4354_-243+4364dup