Canonical Allele Identifier: CA228696434
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs3758987

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113904553T>C , CM000673.2:g.113904553T>C GRCh38
NC_000011.9:g.113775275T>C , CM000673.1:g.113775275T>C GRCh37
NC_000011.8:g.113280485T>C NCBI36
NG_011483.1:g.4687T>C

Transcript Alleles

HGVS Amino-acid change
XM_011543064.1:c.12+5470T>C XP_011541366.1:n.12+5470T>C
XM_024448767.1:c.-242-4742T>C XP_024304535.1:n.-242-4742T>C