Canonical Allele Identifier: CA382769055
Gene: SCN2B HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118039386T>C (hg19) chr11:g.118168671T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118168671T>C , CM000673.2:g.118168671T>C GRCh38
NC_000011.9:g.118039386T>C , CM000673.1:g.118039386T>C GRCh37
NC_000011.8:g.117544596T>C NCBI36
NG_042217.1:g.12952A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000278947.6:c.151A>G MANE Select ENSP00000278947.5:p.Thr51Ala
ENST00000658882.1:c.255A>G ENSP00000499572.1:p.Ala85=
ENST00000665446.1:n.387A>G
ENST00000669850.1:n.393A>G
ENST00000278947.5:c.151A>G ENSP00000278947.5:p.Thr51Ala
NM_004588.4:c.151A>G NP_004579.1:p.Thr51Ala
NM_004588.5:c.151A>G MANE Select NP_004579.1:p.Thr51Ala
Search 100 bp 5'
Search 100 bp 3'