Canonical Allele Identifier: CA671967130
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs1165365998
gnomAD v3: 11-113903446-TTG-T
gnomAD v4: 11-113903446-TTG-T
MyVariant Identifiers: chr11:g.113774169_113774170del (hg19) chr11:g.113903447_113903448del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903447_113903448del , CM000673.2:g.113903447_113903448del GRCh38
NC_000011.9:g.113774169_113774170del , CM000673.1:g.113774169_113774170del GRCh37
NC_000011.8:g.113279379_113279380del NCBI36
NG_011483.1:g.3581_3582del

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4364_12+4365del XP_011541366.1:n.12+4364_12+4365del
XM_024448767.1:c.-243+4364_-243+4365del XP_024304535.1:n.-243+4364_-243+4365del
Search 100 bp 5'
Search 100 bp 3'