Canonical Allele Identifier: CA228695532

Gene: HTR3B

Linked Data

• dbSNP Id: rs930618821
• gnomAD v3: 11-113903423-CTTTTCT-C
• gnomAD v4: 11-113903423-CTTTTCT-C
• MyVariant Identifiers: chr11:g.113774146_113774151del (hg19) ; chr11:g.113903424_113903429del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113903428_113903433del , CM000673.2:g.113903428_113903433del	GRCh38
NC_000011.9:g.113774150_113774155del , CM000673.1:g.113774150_113774155del	GRCh37
NC_000011.8:g.113279360_113279365del	NCBI36
NG_011483.1:g.3562_3567del

Transcript Alleles

HGVS	Amino-acid Change
XM_011543064.1:c.12+4345_12+4350del	XP_011541366.1:n.12+4345_12+4350del
XM_024448767.1:c.-243+4345_-243+4350del	XP_024304535.1:n.-243+4345_-243+4350del