Canonical Allele Identifier: CA379115625

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2465934A>T (hg19) ; chr11:g.2444704A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.19A>T	ENSP00000434560.2:p.Ser7Cys
ENST00000496887.6:c.19A>T	ENSP00000434560.1:p.Ser7Cys