Canonical Allele Identifier: CA2003377700

Gene: SCN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118168127G= , CM000673.2:g.118168127G=	GRCh38
NC_000011.9:g.118038842G= , CM000673.1:g.118038842G=	GRCh37
NC_000011.8:g.117544052G=	NCBI36
NG_042217.1:g.13496C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000278947.6:c.406C= MANE Select	ENSP00000278947.5:p.His136=
ENST00000658882.1:c.*231C=	ENSP00000499572.1:n.*231C=
ENST00000669850.1:n.648C=
ENST00000278947.5:c.406C=	ENSP00000278947.5:p.His136=
NM_004588.4:c.406C=	NP_004579.1:p.His136=
NM_004588.5:c.406C= MANE Select	NP_004579.1:p.His136=