Canonical Allele Identifier: CA379116777
Gene: KCNQ1 HGNC NCBI

Linked Data

gnomAD v4: 11-2445318-C-A
MyVariant Identifiers: chr11:g.2466548C>A (hg19) chr11:g.2445318C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2445318C>A , CM000673.2:g.2445318C>A GRCh38
NC_000011.9:g.2466548C>A , CM000673.1:g.2466548C>A GRCh37
NC_000011.8:g.2423124C>A NCBI36
NG_008935.1:g.5328C>A , LRG_287:g.5328C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.24-65C>A ENSP00000434560.2:n.24-65C>A
ENST00000646564.2:c.220C>A ENSP00000495806.2:p.Pro74Thr
ENST00000155840.12:c.220C>A MANE Select ENSP00000155840.2:p.Pro74Thr
ENST00000155840.9:c.220C>A ENSP00000155840.2:p.Pro74Thr
ENST00000496887.6:c.24-65C>A ENSP00000434560.1:n.24-65C>A
NM_000218.2:c.220C>A , LRG_287t1:c.220C>A NP_000209.2:p.Pro74Thr
NM_000218.3:c.220C>A MANE Select NP_000209.2:p.Pro74Thr
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