Canonical Allele Identifier: CA597114536
Gene: KCNQ1 HGNC NCBI
KCNQ1-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1269540549
gnomAD v2: 11-2870170-G-A
gnomAD v4: 11-2848940-G-A
MyVariant Identifiers: chr11:g.2870170G>A (hg19) chr11:g.2848940G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2848940G>A , CM000673.2:g.2848940G>A GRCh38
NC_000011.9:g.2870170G>A , CM000673.1:g.2870170G>A GRCh37
NC_000011.8:g.2826746G>A NCBI36
NG_008935.1:g.408950G>A , LRG_287:g.408950G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000496887.7:c.*937G>A (KCNQ1) ENSP00000434560.2:n.*937G>A
ENST00000155840.12:c.*937G>A (KCNQ1) MANE Select ENSP00000155840.2:n.*937G>A
ENST00000335475.6:c.*937G>A (KCNQ1) ENSP00000334497.5:n.*937G>A
ENST00000155840.9:c.*937G>A (KCNQ1) ENSP00000155840.2:n.*937G>A
NM_000218.2:c.*937G>A , LRG_287t1:c.*937G>A (KCNQ1) NP_000209.2:n.*937G>A
NM_181798.1:c.*937G>A , LRG_287t2:c.*937G>A (KCNQ1) NP_861463.1:n.*937G>A
NR_130721.1:n.778-8498C>T (KCNQ1-AS1)
NM_000218.3:c.*937G>A (KCNQ1) MANE Select NP_000209.2:n.*937G>A
Search 100 bp 5'
Search 100 bp 3'