Canonical Allele Identifier: CA379115597

Gene: KCNQ1

Linked Data

• MyVariant Identifiers: chr11:g.2465925G>T (hg19) ; chr11:g.2444695G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2444695G>T , CM000673.2:g.2444695G>T	GRCh38
NC_000011.9:g.2465925G>T , CM000673.1:g.2465925G>T	GRCh37
NC_000011.8:g.2422501G>T	NCBI36
NG_008935.1:g.4705G>T , LRG_287:g.4705G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.10G>T	ENSP00000434560.2:p.Ala4Ser
ENST00000496887.6:c.10G>T	ENSP00000434560.1:p.Ala4Ser