Canonical Allele Identifier: CA2003369002

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118143832C= , CM000673.2:g.118143832C=	GRCh38
NC_000011.9:g.118014547C= , CM000673.1:g.118014547C=	GRCh37
NC_000011.8:g.117519757C=	NCBI36
NG_011710.1:g.14084G= , LRG_330:g.14084G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.463+1G= MANE Select	ENSP00000322460.4:n.463+1G=
ENST00000324727.8:c.463+1G=	ENSP00000322460.4:n.463+1G=
ENST00000415030.6:n.606+1G=
ENST00000529878.1:c.62-2496G=	ENSP00000436343.1:n.62-2496G=
ENST00000532138.1:n.719+155G=
NM_001142348.1:c.62-2496G=	NP_001135820.1:n.62-2496G=
NM_001142349.1:c.133+1G=	NP_001135821.1:n.133+1G=
NM_174934.3:c.463+1G= , LRG_330t1:c.463+1G=	NP_777594.1:n.463+1G=
NR_024527.1:n.488+155G=
NM_001142348.2:c.62-2496G=	NP_001135820.1:n.62-2496G=
NM_001142349.2:c.133+1G=	NP_001135821.1:n.133+1G=
NR_024527.2:n.452+155G=
NM_174934.4:c.463+1G= MANE Select	NP_777594.1:n.463+1G=