Canonical Allele Identifier: CA2005869900

Gene: SCN3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123642563C= , CM000673.2:g.123642563C=	GRCh38
NC_000011.9:g.123513271C= , CM000673.1:g.123513271C=	GRCh37
NC_000011.8:g.123018481C=	NCBI36
NG_016283.1:g.17045G= , LRG_421:g.17045G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001040151.2:c.328G= MANE Select	NP_001035241.1:p.Val110=
ENST00000299333.8:c.328G= MANE Select	ENSP00000299333.3:p.Val110=
NM_001040151.1:c.328G=	NP_001035241.1:p.Val110=
NM_018400.3:c.328G= , LRG_421t1:c.328G=	NP_060870.1:p.Val110=
NM_018400.4:c.328G=	NP_060870.1:p.Val110=
ENST00000299333.7:c.328G=	ENSP00000299333.3:p.Val110=
ENST00000392770.6:c.328G=	ENSP00000376523.2:p.Val110=
ENST00000527836.5:c.328G=	ENSP00000435554.1:p.Val110=
ENST00000530277.5:c.328G=	ENSP00000432785.1:p.Val110=
ENST00000657123.1:c.328G=	ENSP00000499439.1:p.Val110=
ENST00000657191.1:c.328G=	ENSP00000499755.1:p.Val110=
ENST00000659826.1:c.24G=
ENST00000667790.1:c.328G=	ENSP00000499234.1:p.Val110=
XM_011542897.1:c.328G=	XP_011541199.1:p.Val110=
XM_011542897.2:c.328G=	XP_011541199.1:p.Val110=
XR_947858.1:n.735G=