Canonical Allele Identifier: CA1948159877
Gene: KCNQ1 HGNC NCBI

Linked Data

dbSNP Id: rs1174214693
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444697G>A , CM000673.2:g.2444697G>A GRCh38
NC_000011.9:g.2465927G>A , CM000673.1:g.2465927G>A GRCh37
NC_000011.8:g.2422503G>A NCBI36
NG_008935.1:g.4707G>A , LRG_287:g.4707G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.12G>A ENSP00000434560.2:p.Ala4=
ENST00000496887.6:c.12G>A ENSP00000434560.1:p.Ala4=
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