Canonical Allele Identifier: CA601784363
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs1213382413

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903327G>A , CM000673.2:g.113903327G>A GRCh38
NC_000011.9:g.113774049G>A , CM000673.1:g.113774049G>A GRCh37
NC_000011.8:g.113279259G>A NCBI36
NG_011483.1:g.3461G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4244G>A XP_011541366.1:n.12+4244G>A
XM_024448767.1:c.-243+4244G>A XP_024304535.1:n.-243+4244G>A