Canonical Allele Identifier: CA2001379826
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs1949709157

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903418_113903423del , CM000673.2:g.113903418_113903423del GRCh38
NC_000011.9:g.113774140_113774145del , CM000673.1:g.113774140_113774145del GRCh37
NC_000011.8:g.113279350_113279355del NCBI36
NG_011483.1:g.3552_3557del

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4335_12+4340del XP_011541366.1:n.12+4335_12+4340del
XM_024448767.1:c.-243+4335_-243+4340del XP_024304535.1:n.-243+4335_-243+4340del