Canonical Allele Identifier: CA2003367906

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141278G= , CM000673.2:g.118141278G=	GRCh38
NC_000011.9:g.118011993G= , CM000673.1:g.118011993G=	GRCh37
NC_000011.8:g.117517203G=	NCBI36
NG_011710.1:g.16638C= , LRG_330:g.16638C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.522C= MANE Select	ENSP00000322460.4:p.Ile174=
ENST00000324727.8:c.522C=	ENSP00000322460.4:p.Ile174=
ENST00000415030.6:n.665C=
ENST00000423160.2:n.156C=
ENST00000529878.1:c.120C=	ENSP00000436343.1:p.Ile40=
ENST00000531550.1:n.587C=
ENST00000532138.1:n.778C=
NM_001142348.1:c.120C=	NP_001135820.1:p.Ile40=
NM_001142349.1:c.192C=	NP_001135821.1:p.Ile64=
NM_174934.3:c.522C= , LRG_330t1:c.522C=	NP_777594.1:p.Ile174=
NR_024527.1:n.547C=
NM_001142348.2:c.120C=	NP_001135820.1:p.Ile40=
NM_001142349.2:c.192C=	NP_001135821.1:p.Ile64=
NR_024527.2:n.511C=
NM_174934.4:c.522C= MANE Select	NP_777594.1:p.Ile174=