Canonical Allele Identifier: CA2001379856

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113903447_113903449delinsTGA , CM000673.2:g.113903447_113903449delinsTGA	GRCh38
NC_000011.9:g.113774169_113774171delinsTGA , CM000673.1:g.113774169_113774171delinsTGA	GRCh37
NC_000011.8:g.113279379_113279381delinsTGA	NCBI36
NG_011483.1:g.3581_3583delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
XM_011543064.1:c.12+4364_12+4366delinsTGA	XP_011541366.1:n.12+4364_12+4366delinsTGA
XM_024448767.1:c.-243+4364_-243+4366delinsTGA	XP_024304535.1:n.-243+4364_-243+4366delinsTGA