Canonical Allele Identifier: CA317447502
Gene: KCNQ2 HGNC NCBI

Linked Data

dbSNP Id: rs118192220
MyVariant Identifiers: chr20:g.62062723C>T (hg19) chr20:g.63431370C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63431370C>T , CM000682.2:g.63431370C>T GRCh38
NC_000020.10:g.62062723C>T , CM000682.1:g.62062723C>T GRCh37
NC_000020.9:g.61533167C>T NCBI36
NG_009004.1:g.46271G>A
NG_009004.2:g.46271G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706989.1:c.1119-1G>A ENSP00000516702.1:n.1119-1G>A
ENST00000359125.7:c.1119-1G>A MANE Select ENSP00000352035.2:n.1119-1G>A
ENST00000636638.1:n.31+2076G>A
ENST00000637193.1:c.599+2439G>A ENSP00000490734.1:n.599+2439G>A
ENST00000344462.8:c.1119-1G>A ENSP00000339611.4:n.1119-1G>A
ENST00000357249.6:c.777-1G>A ENSP00000349789.3:n.777-1G>A
ENST00000359125.6:c.1119-1G>A ENSP00000352035.2:n.1119-1G>A
ENST00000360480.7:c.1118+2439G>A ENSP00000353668.3:n.1118+2439G>A
ENST00000370221.3:n.1245-1G>A
ENST00000370224.5:c.1118+2439G>A ENSP00000359244.2:n.1118+2439G>A
ENST00000625514.2:c.1118+2439G>A ENSP00000486040.1:n.1118+2439G>A
ENST00000626839.2:c.1119-1G>A ENSP00000486706.1:n.1119-1G>A
ENST00000627221.2:c.262+2439G>A
ENST00000629241.2:c.1118+2439G>A ENSP00000487142.1:n.1118+2439G>A
ENST00000629676.2:c.1118+2439G>A ENSP00000486194.1:n.1118+2439G>A
NM_004518.4:c.1118+2439G>A NP_004509.2:n.1118+2439G>A
NM_172106.1:c.1119-1G>A NP_742104.1:n.1119-1G>A
NM_172107.2:c.1119-1G>A NP_742105.1:n.1119-1G>A
NM_172108.3:c.1119-1G>A NP_742106.1:n.1119-1G>A
XM_006723787.1:c.1119-1G>A XP_006723850.1:n.1119-1G>A
XM_011528807.1:c.1119-1G>A XP_011527109.1:n.1119-1G>A
XM_011528808.1:c.1119-1G>A XP_011527110.1:n.1119-1G>A
XM_011528809.1:c.1118+2439G>A XP_011527111.1:n.1118+2439G>A
XM_011528810.1:c.1119-1G>A XP_011527112.1:n.1119-1G>A
XM_011528811.1:c.1118+2439G>A XP_011527113.1:n.1118+2439G>A
XM_011528812.1:c.1119-1G>A XP_011527114.1:n.1119-1G>A
XM_011528813.1:c.993-1G>A XP_011527115.1:n.993-1G>A
XM_011528814.1:c.600-1G>A XP_011527116.1:n.600-1G>A
XM_011528815.1:c.1119-1G>A XP_011527117.1:n.1119-1G>A
NM_004518.5:c.1118+2439G>A NP_004509.2:n.1118+2439G>A
NM_172106.2:c.1119-1G>A NP_742104.1:n.1119-1G>A
NM_172107.3:c.1119-1G>A NP_742105.1:n.1119-1G>A
NM_172108.4:c.1119-1G>A NP_742106.1:n.1119-1G>A
XM_011528810.2:c.1119-1G>A XP_011527112.1:n.1119-1G>A
XM_011528811.2:c.1118+2439G>A XP_011527113.1:n.1118+2439G>A
XM_017027841.2:c.1119-1G>A XP_016883330.1:n.1119-1G>A
XM_017027842.2:c.1119-1G>A XP_016883331.1:n.1119-1G>A
XM_017027843.1:c.1050-1G>A XP_016883332.1:n.1050-1G>A
XM_017027844.2:c.1119-1G>A XP_016883333.1:n.1119-1G>A
NM_004518.6:c.1118+2439G>A NP_004509.2:n.1118+2439G>A
NM_172106.3:c.1119-1G>A NP_742104.1:n.1119-1G>A
NM_172107.4:c.1119-1G>A MANE Select NP_742105.1:n.1119-1G>A
NM_172108.5:c.1119-1G>A NP_742106.1:n.1119-1G>A
NM_001382235.1:c.1119-1G>A NP_001369164.1:n.1119-1G>A
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