Canonical Allele Identifier: CA2003369038

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118143919G= , CM000673.2:g.118143919G=	GRCh38
NC_000011.9:g.118014634G= , CM000673.1:g.118014634G=	GRCh37
NC_000011.8:g.117519844G=	NCBI36
NG_011710.1:g.13997C= , LRG_330:g.13997C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.377C= MANE Select	ENSP00000322460.4:p.Thr126=
ENST00000324727.8:c.377C=	ENSP00000322460.4:p.Thr126=
ENST00000415030.6:n.520C=
ENST00000529878.1:c.62-2583C=	ENSP00000436343.1:n.62-2583C=
ENST00000532138.1:n.719+68C=
NM_001142348.1:c.62-2583C=	NP_001135820.1:n.62-2583C=
NM_001142349.1:c.47C=	NP_001135821.1:p.Thr16=
NM_174934.3:c.377C= , LRG_330t1:c.377C=	NP_777594.1:p.Thr126=
NR_024527.1:n.488+68C=
NM_001142348.2:c.62-2583C=	NP_001135820.1:n.62-2583C=
NM_001142349.2:c.47C=	NP_001135821.1:p.Thr16=
NR_024527.2:n.452+68C=
NM_174934.4:c.377C= MANE Select	NP_777594.1:p.Thr126=