Canonical Allele Identifier: CA942403908
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs1949709253

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903428_113903437del , CM000673.2:g.113903428_113903437del GRCh38
NC_000011.9:g.113774150_113774159del , CM000673.1:g.113774150_113774159del GRCh37
NC_000011.8:g.113279360_113279369del NCBI36
NG_011483.1:g.3562_3571del

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4345_12+4354del XP_011541366.1:n.12+4345_12+4354del
XM_024448767.1:c.-243+4345_-243+4354del XP_024304535.1:n.-243+4345_-243+4354del