Canonical Allele Identifier: CA16620820

Gene: SCN1B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35030833C>A , CM000681.2:g.35030833C>A	GRCh38
NC_000019.9:g.35521737C>A , CM000681.1:g.35521737C>A	GRCh37
NC_000019.8:g.40213577C>A	NCBI36
NG_013359.1:g.5146C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001037.5:c.13C>A MANE Select	NP_001028.1:p.Leu5Met
ENST00000262631.11:c.13C>A MANE Select	ENSP00000262631.3:p.Leu5Met
NM_001037.4:c.13C>A	NP_001028.1:p.Leu5Met
NM_199037.3:c.13C>A	NP_950238.1:p.Leu5Met
NM_199037.4:c.13C>A	NP_950238.1:p.Leu5Met
NM_199037.5:c.13C>A	NP_950238.1:p.Leu5Met
ENST00000262631.9:c.13C>A	ENSP00000262631.3:p.Leu5Met
ENST00000415950.3:c.13C>A	ENSP00000396915.2:p.Leu5Met
ENST00000415950.4:c.13C>A	ENSP00000396915.2:p.Leu5Met
ENST00000415950.5:c.13C>A	ENSP00000396915.2:p.Leu5Met
ENST00000595652.5:c.13C>A	ENSP00000468848.1:p.Leu5Met
ENST00000638536.1:c.13C>A	ENSP00000492022.1:p.Leu5Met