Canonical Allele Identifier: CA674857800

Gene: KCNQ1

Linked Data

• dbSNP Id: rs1487032440
• gnomAD v3: 11-2444925-G-C
• gnomAD v4: 11-2444925-G-C
• MyVariant Identifiers: chr11:g.2466155G>C (hg19) ; chr11:g.2444925G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2444925G>C , CM000673.2:g.2444925G>C	GRCh38
NC_000011.9:g.2466155G>C , CM000673.1:g.2466155G>C	GRCh37
NC_000011.8:g.2422731G>C	NCBI36
NG_008935.1:g.4935G>C , LRG_287:g.4935G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496887.7:c.23+217G>C	ENSP00000434560.2:n.23+217G>C
ENST00000496887.6:c.23+217G>C	ENSP00000434560.1:n.23+217G>C