Canonical Allele Identifier: CA674857796
Gene: KCNQ1 HGNC NCBI

Linked Data

dbSNP Id: rs1424658253
MyVariant Identifiers: chr11:g.2466148T>C (hg19) chr11:g.2444918T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444918T>C , CM000673.2:g.2444918T>C GRCh38
NC_000011.9:g.2466148T>C , CM000673.1:g.2466148T>C GRCh37
NC_000011.8:g.2422724T>C NCBI36
NG_008935.1:g.4928T>C , LRG_287:g.4928T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.23+210T>C ENSP00000434560.2:n.23+210T>C
ENST00000496887.6:c.23+210T>C ENSP00000434560.1:n.23+210T>C
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