Canonical Allele Identifier: CA2003367913

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141288C= , CM000673.2:g.118141288C=	GRCh38
NC_000011.9:g.118012003C= , CM000673.1:g.118012003C=	GRCh37
NC_000011.8:g.117517213C=	NCBI36
NG_011710.1:g.16628G= , LRG_330:g.16628G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.512G= MANE Select	ENSP00000322460.4:p.Gly171=
ENST00000324727.8:c.512G=	ENSP00000322460.4:p.Gly171=
ENST00000415030.6:n.655G=
ENST00000423160.2:n.146G=
ENST00000529878.1:c.110G=	ENSP00000436343.1:p.Gly37=
ENST00000531550.1:n.577G=
ENST00000532138.1:n.768G=
NM_001142348.1:c.110G=	NP_001135820.1:p.Gly37=
NM_001142349.1:c.182G=	NP_001135821.1:p.Gly61=
NM_174934.3:c.512G= , LRG_330t1:c.512G=	NP_777594.1:p.Gly171=
NR_024527.1:n.537G=
NM_001142348.2:c.110G=	NP_001135820.1:p.Gly37=
NM_001142349.2:c.182G=	NP_001135821.1:p.Gly61=
NR_024527.2:n.501G=
NM_174934.4:c.512G= MANE Select	NP_777594.1:p.Gly171=