Canonical Allele Identifier: CA674857671
Gene: KCNQ1 HGNC NCBI

Linked Data

dbSNP Id: rs1394683892
gnomAD v3: 11-2444791-G-T
gnomAD v4: 11-2444791-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444791G>T , CM000673.2:g.2444791G>T GRCh38
NC_000011.9:g.2466021G>T , CM000673.1:g.2466021G>T GRCh37
NC_000011.8:g.2422597G>T NCBI36
NG_008935.1:g.4801G>T , LRG_287:g.4801G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.23+83G>T ENSP00000434560.2:n.23+83G>T
ENST00000496887.6:c.23+83G>T ENSP00000434560.1:n.23+83G>T