Canonical Allele Identifier: CA2003367933

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141331C= , CM000673.2:g.118141331C=	GRCh38
NC_000011.9:g.118012046C= , CM000673.1:g.118012046C=	GRCh37
NC_000011.8:g.117517256C=	NCBI36
NG_011710.1:g.16585G= , LRG_330:g.16585G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324727.9:c.469G= MANE Select	ENSP00000322460.4:p.Glu157=
ENST00000324727.8:c.469G=	ENSP00000322460.4:p.Glu157=
ENST00000415030.6:n.612G=
ENST00000423160.2:n.103G=
ENST00000529878.1:c.67G=	ENSP00000436343.1:p.Glu23=
ENST00000531550.1:n.534G=
ENST00000532138.1:n.725G=
NM_001142348.1:c.67G=	NP_001135820.1:p.Glu23=
NM_001142349.1:c.139G=	NP_001135821.1:p.Glu47=
NM_174934.3:c.469G= , LRG_330t1:c.469G=	NP_777594.1:p.Glu157=
NR_024527.1:n.494G=
NM_001142348.2:c.67G=	NP_001135820.1:p.Glu23=
NM_001142349.2:c.139G=	NP_001135821.1:p.Glu47=
NR_024527.2:n.458G=
NM_174934.4:c.469G= MANE Select	NP_777594.1:p.Glu157=