Canonical Allele Identifier: CA1948160130
Gene: KCNQ1 HGNC NCBI

Linked Data

dbSNP Id: rs1846004696
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444799G>C , CM000673.2:g.2444799G>C GRCh38
NC_000011.9:g.2466029G>C , CM000673.1:g.2466029G>C GRCh37
NC_000011.8:g.2422605G>C NCBI36
NG_008935.1:g.4809G>C , LRG_287:g.4809G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.23+91G>C ENSP00000434560.2:n.23+91G>C
ENST00000496887.6:c.23+91G>C ENSP00000434560.1:n.23+91G>C
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