Canonical Allele Identifier: CA2001379784
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs1949708501

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903326G>C , CM000673.2:g.113903326G>C GRCh38
NC_000011.9:g.113774048G>C , CM000673.1:g.113774048G>C GRCh37
NC_000011.8:g.113279258G>C NCBI36
NG_011483.1:g.3460G>C

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4243G>C XP_011541366.1:n.12+4243G>C
XM_024448767.1:c.-243+4243G>C XP_024304535.1:n.-243+4243G>C