Canonical Allele Identifier: CA477080571

Gene: SCN2B

Linked Data

• MyVariant Identifiers: chr11:g.118039414G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118168699G>A , CM000673.2:g.118168699G>A	GRCh38
NC_000011.9:g.118039414G>A , CM000673.1:g.118039414G>A	GRCh37
NC_000011.8:g.117544624G>A	NCBI36
NG_042217.1:g.12924C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278947.6:c.123C>T MANE Select	ENSP00000278947.5:p.Leu41=
ENST00000658882.1:c.227C>T	ENSP00000499572.1:p.Ser76Leu
ENST00000665446.1:n.359C>T
ENST00000669850.1:n.365C>T
ENST00000278947.5:c.123C>T	ENSP00000278947.5:p.Leu41=
NM_004588.4:c.123C>T	NP_004579.1:p.Leu41=
NM_004588.5:c.123C>T MANE Select	NP_004579.1:p.Leu41=