Canonical Allele Identifier: CA2003367947

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141369C= , CM000673.2:g.118141369C=	GRCh38
NC_000011.9:g.118012084C= , CM000673.1:g.118012084C=	GRCh37
NC_000011.8:g.117517294C=	NCBI36
NG_011710.1:g.16547G= , LRG_330:g.16547G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.464-33G= MANE Select	ENSP00000322460.4:n.464-33G=
ENST00000324727.8:c.464-33G=	ENSP00000322460.4:n.464-33G=
ENST00000415030.6:n.607-33G=
ENST00000423160.2:n.98-33G=
ENST00000529878.1:c.62-33G=	ENSP00000436343.1:n.62-33G=
ENST00000531550.1:n.496G=
ENST00000532138.1:n.720-33G=
NM_001142348.1:c.62-33G=	NP_001135820.1:n.62-33G=
NM_001142349.1:c.134-33G=	NP_001135821.1:n.134-33G=
NM_174934.3:c.464-33G= , LRG_330t1:c.464-33G=	NP_777594.1:n.464-33G=
NR_024527.1:n.489-33G=
NM_001142348.2:c.62-33G=	NP_001135820.1:n.62-33G=
NM_001142349.2:c.134-33G=	NP_001135821.1:n.134-33G=
NR_024527.2:n.453-33G=
NM_174934.4:c.464-33G= MANE Select	NP_777594.1:n.464-33G=