Canonical Allele Identifier: CA601784375

Gene: HTR3B

Linked Data

• gnomAD v2: 11-113774153-T-TC
• MyVariant Identifiers: chr11:g.113774153_113774154insC (hg19) ; chr11:g.113903431_113903432insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113903431_113903432insC , CM000673.2:g.113903431_113903432insC	GRCh38
NC_000011.9:g.113774153_113774154insC , CM000673.1:g.113774153_113774154insC	GRCh37
NC_000011.8:g.113279363_113279364insC	NCBI36
NG_011483.1:g.3565_3566insC

Transcript Alleles

HGVS	Amino-acid Change
XM_011543064.1:c.12+4348_12+4349insC	XP_011541366.1:n.12+4348_12+4349insC
XM_024448767.1:c.-243+4348_-243+4349insC	XP_024304535.1:n.-243+4348_-243+4349insC