Canonical Allele Identifier: CA2003367892

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141251G= , CM000673.2:g.118141251G=	GRCh38
NC_000011.9:g.118011966G= , CM000673.1:g.118011966G=	GRCh37
NC_000011.8:g.117517176G=	NCBI36
NG_011710.1:g.16665C= , LRG_330:g.16665C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.549C= MANE Select	ENSP00000322460.4:p.Ile183=
ENST00000324727.8:c.549C=	ENSP00000322460.4:p.Ile183=
ENST00000415030.6:n.692C=
ENST00000423160.2:n.183C=
ENST00000529878.1:c.147C=	ENSP00000436343.1:p.Ile49=
ENST00000531550.1:n.614C=
ENST00000532138.1:n.805C=
NM_001142348.1:c.147C=	NP_001135820.1:p.Ile49=
NM_001142349.1:c.219C=	NP_001135821.1:p.Ile73=
NM_174934.3:c.549C= , LRG_330t1:c.549C=	NP_777594.1:p.Ile183=
NR_024527.1:n.574C=
NM_001142348.2:c.147C=	NP_001135820.1:p.Ile49=
NM_001142349.2:c.219C=	NP_001135821.1:p.Ile73=
NR_024527.2:n.538C=
NM_174934.4:c.549C= MANE Select	NP_777594.1:p.Ile183=