Canonical Allele Identifier: CA2003367908

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141282A= , CM000673.2:g.118141282A=	GRCh38
NC_000011.9:g.118011997A= , CM000673.1:g.118011997A=	GRCh37
NC_000011.8:g.117517207A=	NCBI36
NG_011710.1:g.16634T= , LRG_330:g.16634T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.518T= MANE Select	ENSP00000322460.4:p.Val173=
ENST00000324727.8:c.518T=	ENSP00000322460.4:p.Val173=
ENST00000415030.6:n.661T=
ENST00000423160.2:n.152T=
ENST00000529878.1:c.116T=	ENSP00000436343.1:p.Val39=
ENST00000531550.1:n.583T=
ENST00000532138.1:n.774T=
NM_001142348.1:c.116T=	NP_001135820.1:p.Val39=
NM_001142349.1:c.188T=	NP_001135821.1:p.Val63=
NM_174934.3:c.518T= , LRG_330t1:c.518T=	NP_777594.1:p.Val173=
NR_024527.1:n.543T=
NM_001142348.2:c.116T=	NP_001135820.1:p.Val39=
NM_001142349.2:c.188T=	NP_001135821.1:p.Val63=
NR_024527.2:n.507T=
NM_174934.4:c.518T= MANE Select	NP_777594.1:p.Val173=