Canonical Allele Identifier: CA2003367918

Gene: SCN4B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141298C= , CM000673.2:g.118141298C=	GRCh38
NC_000011.9:g.118012013C= , CM000673.1:g.118012013C=	GRCh37
NC_000011.8:g.117517223C=	NCBI36
NG_011710.1:g.16618G= , LRG_330:g.16618G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.502G= MANE Select	ENSP00000322460.4:p.Ala168=
ENST00000324727.8:c.502G=	ENSP00000322460.4:p.Ala168=
ENST00000415030.6:n.645G=
ENST00000423160.2:n.136G=
ENST00000529878.1:c.100G=	ENSP00000436343.1:p.Ala34=
ENST00000531550.1:n.567G=
ENST00000532138.1:n.758G=
NM_001142348.1:c.100G=	NP_001135820.1:p.Ala34=
NM_001142349.1:c.172G=	NP_001135821.1:p.Ala58=
NM_174934.3:c.502G= , LRG_330t1:c.502G=	NP_777594.1:p.Ala168=
NR_024527.1:n.527G=
NM_001142348.2:c.100G=	NP_001135820.1:p.Ala34=
NM_001142349.2:c.172G=	NP_001135821.1:p.Ala58=
NR_024527.2:n.491G=
NM_174934.4:c.502G= MANE Select	NP_777594.1:p.Ala168=