Canonical Allele Identifier: CA2003366034

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118137122T= , CM000673.2:g.118137122T=	GRCh38
NC_000011.9:g.118007837T= , CM000673.1:g.118007837T=	GRCh37
NC_000011.8:g.117513047T=	NCBI36
NG_011710.1:g.20794A= , LRG_330:g.20794A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000324727.9:c.594-2A= MANE Select	ENSP00000322460.4:n.594-2A=
ENST00000324727.8:c.594-2A=	ENSP00000322460.4:n.594-2A=
ENST00000415030.6:n.737-2A=
ENST00000423160.2:n.228-2A=
ENST00000529878.1:c.192-2A=	ENSP00000436343.1:n.192-2A=
ENST00000531550.1:n.659-2A=
NM_001142348.1:c.192-2A=	NP_001135820.1:n.192-2A=
NM_001142349.1:c.264-2A=	NP_001135821.1:n.264-2A=
NM_174934.3:c.594-2A= , LRG_330t1:c.594-2A=	NP_777594.1:n.594-2A=
NR_024527.1:n.619-2A=
NM_001142348.2:c.192-2A=	NP_001135820.1:n.192-2A=
NM_001142349.2:c.264-2A=	NP_001135821.1:n.264-2A=
NR_024527.2:n.583-2A=
NM_174934.4:c.594-2A= MANE Select	NP_777594.1:n.594-2A=