Canonical Allele Identifier: CA379115623
Gene: KCNQ1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.2465934A>G (hg19) chr11:g.2444704A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444704A>G , CM000673.2:g.2444704A>G GRCh38
NC_000011.9:g.2465934A>G , CM000673.1:g.2465934A>G GRCh37
NC_000011.8:g.2422510A>G NCBI36
NG_008935.1:g.4714A>G , LRG_287:g.4714A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000496887.7:c.19A>G ENSP00000434560.2:p.Ser7Gly
ENST00000496887.6:c.19A>G ENSP00000434560.1:p.Ser7Gly
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