Canonical Allele Identifier: CA2333466353

Gene: SCN1B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35032065A= , CM000681.2:g.35032065A=	GRCh38
NC_000019.9:g.35522969A= , CM000681.1:g.35522969A=	GRCh37
NC_000019.8:g.40214809A=	NCBI36
NG_013359.1:g.6378A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415950.5:c.41-463A=	ENSP00000396915.2:n.41-463A=
ENST00000262631.11:c.41-463A= MANE Select	ENSP00000262631.3:n.41-463A=
ENST00000415950.4:c.41-463A=	ENSP00000396915.2:n.41-463A=
ENST00000596348.2:c.-60+285A=	ENSP00000492247.1:n.-60+285A=
ENST00000638536.1:c.41-463A=	ENSP00000492022.1:n.41-463A=
ENST00000640135.1:c.-60+285A=	ENSP00000492655.1:n.-60+285A=
ENST00000262631.9:c.41-463A=	ENSP00000262631.3:n.41-463A=
ENST00000415950.3:c.41-463A=	ENSP00000396915.2:n.41-463A=
ENST00000595652.5:c.41-463A=	ENSP00000468848.1:n.41-463A=
ENST00000596348.1:n.49+285A=
NM_001037.4:c.41-463A=	NP_001028.1:n.41-463A=
NM_199037.3:c.41-463A=	NP_950238.1:n.41-463A=
XM_005259144.1:c.-60+285A=	XP_005259201.1:n.-60+285A=
NM_001321605.1:c.-60+285A=	NP_001308534.1:n.-60+285A=
NM_199037.4:c.41-463A=	NP_950238.1:n.41-463A=
NM_001037.5:c.41-463A= MANE Select	NP_001028.1:n.41-463A=
NM_001321605.2:c.-60+285A=	NP_001308534.1:n.-60+285A=
NM_199037.5:c.41-463A=	NP_950238.1:n.41-463A=