Canonical Allele Identifier: CA16617256
Gene: SCN2A HGNC NCBI

Linked Data

ClinVar Variation Id: 422127
ClinVar RCV Id: RCV000484885
dbSNP Id: rs1064795576
MyVariant Identifiers: chr2:g.166153564G>A (hg19) chr2:g.165297054G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165297054G>A , CM000664.2:g.165297054G>A GRCh38
NC_000002.11:g.166153564G>A , CM000664.1:g.166153564G>A GRCh37
NC_000002.10:g.165861810G>A NCBI36
NG_008143.1:g.62653G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000631182.3:c.305G>A MANE Plus Clinical ENSP00000486885.1:p.Arg102Gln
ENST00000375437.7:c.305G>A MANE Select ENSP00000364586.2:p.Arg102Gln
ENST00000635945.1:n.668G>A
ENST00000636071.2:c.305G>A ENSP00000490107.1:p.Arg102Gln
ENST00000636135.1:c.305G>A ENSP00000489821.1:p.Arg102Gln
ENST00000636384.2:c.305G>A ENSP00000490765.1:p.Arg102Gln
ENST00000636662.2:c.*828G>A ENSP00000489873.1:n.*828G>A
ENST00000636769.1:c.305G>A ENSP00000490800.1:p.Arg102Gln
ENST00000636985.2:c.-92G>A ENSP00000490849.1:n.-92G>A
ENST00000637266.2:c.305G>A ENSP00000490866.1:p.Arg102Gln
ENST00000637367.1:c.*238G>A ENSP00000490592.1:n.*238G>A
ENST00000638151.1:n.389G>A
ENST00000283256.10:c.305G>A ENSP00000283256.6:p.Arg102Gln
ENST00000375427.4:c.305G>A ENSP00000364576.2:p.Arg102Gln
ENST00000375437.6:c.305G>A ENSP00000364586.2:p.Arg102Gln
ENST00000424833.5:c.305G>A ENSP00000406454.2:p.Arg102Gln
ENST00000480032.4:n.448G>A
ENST00000631182.2:c.305G>A ENSP00000486885.1:p.Arg102Gln
NM_001040142.1:c.305G>A NP_001035232.1:p.Arg102Gln
NM_001040143.1:c.305G>A NP_001035233.1:p.Arg102Gln
NM_021007.2:c.305G>A NP_066287.2:p.Arg102Gln
XM_005246750.2:c.305G>A XP_005246807.1:p.Arg102Gln
XM_005246753.2:c.305G>A XP_005246810.1:p.Arg102Gln
XM_005246754.3:c.275G>A XP_005246811.1:p.Arg92Gln
XM_011511608.1:c.305G>A XP_011509910.1:p.Arg102Gln
XM_011511609.1:c.305G>A XP_011509911.1:p.Arg102Gln
XM_005246753.3:c.305G>A XP_005246810.1:p.Arg102Gln
XM_017004656.1:c.305G>A XP_016860145.1:p.Arg102Gln
XM_017004657.1:c.305G>A XP_016860146.1:p.Arg102Gln
XM_017004658.1:c.-636G>A XP_016860147.1:n.-636G>A
XM_024453037.1:c.-357G>A XP_024308805.1:n.-357G>A
NM_001040142.2:c.305G>A MANE Select NP_001035232.1:p.Arg102Gln
NM_001040143.2:c.305G>A NP_001035233.1:p.Arg102Gln
NM_001371246.1:c.305G>A MANE Plus Clinical NP_001358175.1:p.Arg102Gln
NM_001371247.1:c.305G>A NP_001358176.1:p.Arg102Gln
NM_021007.3:c.305G>A NP_066287.2:p.Arg102Gln
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