Canonical Allele Identifier: CA476834680
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs1185155120
gnomAD v3: 11-113903427-TC-T
gnomAD v4: 11-113903427-TC-T
MyVariant Identifiers: chr11:g.113774150del (hg19) chr11:g.113903428del (hg38)
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Genomic Alleles

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

Transcript Alleles

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