Canonical Allele Identifier: CA2003366016

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118137097G= , CM000673.2:g.118137097G=	GRCh38
NC_000011.9:g.118007812G= , CM000673.1:g.118007812G=	GRCh37
NC_000011.8:g.117513022G=	NCBI36
NG_011710.1:g.20819C= , LRG_330:g.20819C=

Transcript Alleles

HGVS	Amino-acid Change
NM_174934.4:c.617C= MANE Select	NP_777594.1:p.Ser206=
ENST00000324727.9:c.617C= MANE Select	ENSP00000322460.4:p.Ser206=
NM_001142348.1:c.215C=	NP_001135820.1:p.Ser72=
NM_001142348.2:c.215C=	NP_001135820.1:p.Ser72=
NM_001142349.1:c.287C=	NP_001135821.1:p.Ser96=
NM_001142349.2:c.287C=	NP_001135821.1:p.Ser96=
NM_174934.3:c.617C= , LRG_330t1:c.617C=	NP_777594.1:p.Ser206=
NR_024527.1:n.642C=
NR_024527.2:n.606C=
ENST00000324727.8:c.617C=	ENSP00000322460.4:p.Ser206=
ENST00000415030.6:n.760C=
ENST00000423160.2:n.251C=
ENST00000529878.1:c.215C=	ENSP00000436343.1:p.Ser72=
ENST00000531550.1:n.682C=