Canonical Allele Identifier: CA2003369007

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118143841A= , CM000673.2:g.118143841A=	GRCh38
NC_000011.9:g.118014556A= , CM000673.1:g.118014556A=	GRCh37
NC_000011.8:g.117519766A=	NCBI36
NG_011710.1:g.14075T= , LRG_330:g.14075T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.455T= MANE Select	ENSP00000322460.4:p.Val152=
ENST00000324727.8:c.455T=	ENSP00000322460.4:p.Val152=
ENST00000415030.6:n.598T=
ENST00000529878.1:c.62-2505T=	ENSP00000436343.1:n.62-2505T=
ENST00000532138.1:n.719+146T=
NM_001142348.1:c.62-2505T=	NP_001135820.1:n.62-2505T=
NM_001142349.1:c.125T=	NP_001135821.1:p.Val42=
NM_174934.3:c.455T= , LRG_330t1:c.455T=	NP_777594.1:p.Val152=
NR_024527.1:n.488+146T=
NM_001142348.2:c.62-2505T=	NP_001135820.1:n.62-2505T=
NM_001142349.2:c.125T=	NP_001135821.1:p.Val42=
NR_024527.2:n.452+146T=
NM_174934.4:c.455T= MANE Select	NP_777594.1:p.Val152=