Canonical Allele Identifier: CA674857492
Gene: KCNQ1 HGNC NCBI

Linked Data

dbSNP Id: rs1455158510
gnomAD v3: 11-2444668-C-CG
gnomAD v4: 11-2444668-C-CG
MyVariant Identifiers: chr11:g.2465898_2465899insG (hg19) chr11:g.2444668_2444669insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444672dup , CM000673.2:g.2444672dup GRCh38
NC_000011.9:g.2465902dup , CM000673.1:g.2465902dup GRCh37
NC_000011.8:g.2422478dup NCBI36
NG_008935.1:g.4682dup , LRG_287:g.4682dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.-14dup ENSP00000434560.2:n.-14dup
Search 100 bp 5'
Search 100 bp 3'