Canonical Allele Identifier: CA2003367935

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141334C= , CM000673.2:g.118141334C=	GRCh38
NC_000011.9:g.118012049C= , CM000673.1:g.118012049C=	GRCh37
NC_000011.8:g.117517259C=	NCBI36
NG_011710.1:g.16582G= , LRG_330:g.16582G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.466G= MANE Select	ENSP00000322460.4:p.Glu156=
ENST00000324727.8:c.466G=	ENSP00000322460.4:p.Glu156=
ENST00000415030.6:n.609G=
ENST00000423160.2:n.100G=
ENST00000529878.1:c.64G=	ENSP00000436343.1:p.Glu22=
ENST00000531550.1:n.531G=
ENST00000532138.1:n.722G=
NM_001142348.1:c.64G=	NP_001135820.1:p.Glu22=
NM_001142349.1:c.136G=	NP_001135821.1:p.Glu46=
NM_174934.3:c.466G= , LRG_330t1:c.466G=	NP_777594.1:p.Glu156=
NR_024527.1:n.491G=
NM_001142348.2:c.64G=	NP_001135820.1:p.Glu22=
NM_001142349.2:c.136G=	NP_001135821.1:p.Glu46=
NR_024527.2:n.455G=
NM_174934.4:c.466G= MANE Select	NP_777594.1:p.Glu156=