Canonical Allele Identifier: CA2003367927

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141315A= , CM000673.2:g.118141315A=	GRCh38
NC_000011.9:g.118012030A= , CM000673.1:g.118012030A=	GRCh37
NC_000011.8:g.117517240A=	NCBI36
NG_011710.1:g.16601T= , LRG_330:g.16601T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.485T= MANE Select	ENSP00000322460.4:p.Val162=
ENST00000324727.8:c.485T=	ENSP00000322460.4:p.Val162=
ENST00000415030.6:n.628T=
ENST00000423160.2:n.119T=
ENST00000529878.1:c.83T=	ENSP00000436343.1:p.Val28=
ENST00000531550.1:n.550T=
ENST00000532138.1:n.741T=
NM_001142348.1:c.83T=	NP_001135820.1:p.Val28=
NM_001142349.1:c.155T=	NP_001135821.1:p.Val52=
NM_174934.3:c.485T= , LRG_330t1:c.485T=	NP_777594.1:p.Val162=
NR_024527.1:n.510T=
NM_001142348.2:c.83T=	NP_001135820.1:p.Val28=
NM_001142349.2:c.155T=	NP_001135821.1:p.Val52=
NR_024527.2:n.474T=
NM_174934.4:c.485T= MANE Select	NP_777594.1:p.Val162=