Canonical Allele Identifier: CA2003378000

Gene: SCN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118168724G= , CM000673.2:g.118168724G=	GRCh38
NC_000011.9:g.118039439G= , CM000673.1:g.118039439G=	GRCh37
NC_000011.8:g.117544649G=	NCBI36
NG_042217.1:g.12899C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278947.6:c.98C= MANE Select	ENSP00000278947.5:p.Thr33=
ENST00000658882.1:c.202C=	ENSP00000499572.1:p.Gln68=
ENST00000665446.1:n.334C=
ENST00000669850.1:n.340C=
ENST00000278947.5:c.98C=	ENSP00000278947.5:p.Thr33=
NM_004588.4:c.98C=	NP_004579.1:p.Thr33=
NM_004588.5:c.98C= MANE Select	NP_004579.1:p.Thr33=