Canonical Allele Identifier: CA2003367932

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141325C= , CM000673.2:g.118141325C=	GRCh38
NC_000011.9:g.118012040C= , CM000673.1:g.118012040C=	GRCh37
NC_000011.8:g.117517250C=	NCBI36
NG_011710.1:g.16591G= , LRG_330:g.16591G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324727.9:c.475G= MANE Select	ENSP00000322460.4:p.Asp159=
ENST00000324727.8:c.475G=	ENSP00000322460.4:p.Asp159=
ENST00000415030.6:n.618G=
ENST00000423160.2:n.109G=
ENST00000529878.1:c.73G=	ENSP00000436343.1:p.Asp25=
ENST00000531550.1:n.540G=
ENST00000532138.1:n.731G=
NM_001142348.1:c.73G=	NP_001135820.1:p.Asp25=
NM_001142349.1:c.145G=	NP_001135821.1:p.Asp49=
NM_174934.3:c.475G= , LRG_330t1:c.475G=	NP_777594.1:p.Asp159=
NR_024527.1:n.500G=
NM_001142348.2:c.73G=	NP_001135820.1:p.Asp25=
NM_001142349.2:c.145G=	NP_001135821.1:p.Asp49=
NR_024527.2:n.464G=
NM_174934.4:c.475G= MANE Select	NP_777594.1:p.Asp159=