Canonical Allele Identifier: CA11036088
Gene: SCN2A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10184275

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.165271418G>A , CM000664.2:g.165271418G>A GRCh38
NC_000002.11:g.166127928G>A , CM000664.1:g.166127928G>A GRCh37
NC_000002.10:g.165836174G>A NCBI36
NG_008143.1:g.37017G>A

Transcript Alleles

HGVS Amino-acid change
NM_001040142.1:c.-51-24355G>A VV NP_001035232.1:p.=
XM_005246750.2:c.-51-24355G>A XP_005246807.1:p.=
XM_005246753.2:c.-51-24355G>A XP_005246810.1:p.=
XM_005246754.3:c.27-24462G>A XP_005246811.1:p.=
XM_011511608.1:c.-51-24355G>A XP_011509910.1:p.=
XM_011511609.1:c.-51-24355G>A XP_011509911.1:p.=
XM_005246753.3:c.-51-24355G>A
XM_017004656.1:c.-51-24355G>A XP_016860145.1:p.=
XM_017004658.1:c.-991-24355G>A XP_016860147.1:p.=
XM_024453037.1:c.-712-24355G>A XP_024308805.1:p.=
NM_001040142.2:c.-51-24355G>A VV MANE Preferred
ENST00000375437.6:c.-51-24355G>A ENSP00000364586.2:p.=
ENST00000424833.5:c.-51-24355G>A ENSP00000406454.2:p.=
ENST00000631182.2:c.-51-24355G>A ENSP00000486885.1:p.=