Canonical Allele Identifier: CA2333466994
Gene: SCN1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35033556C= , CM000681.2:g.35033556C= GRCh38
NC_000019.9:g.35524460C= , CM000681.1:g.35524460C= GRCh37
NC_000019.8:g.40216300C= NCBI36
NG_013359.1:g.7869C=

Transcript Alleles

HGVS Amino-acid change
ENST00000415950.5:c.265C= ENSP00000396915.2:p.Arg89=
ENST00000262631.11:c.265C= MANE Select ENSP00000262631.3:p.Arg89=
ENST00000415950.4:c.265C= ENSP00000396915.2:p.Arg89=
ENST00000596348.2:c.166C= ENSP00000492247.1:p.Arg56=
ENST00000638536.1:c.265C= ENSP00000492022.1:p.Arg89=
ENST00000640135.1:c.166C= ENSP00000492655.1:p.Arg56=
ENST00000675741.1:c.166C= ENSP00000502395.1:p.Arg56=
ENST00000676410.1:c.166C= ENSP00000502717.1:p.Arg56=
ENST00000262631.9:c.265C= ENSP00000262631.3:p.Arg89=
ENST00000415950.3:c.265C= ENSP00000396915.2:p.Arg89=
ENST00000595652.5:c.208-156C= ENSP00000468848.1:n.208-156C=
ENST00000596348.1:n.274C=
NM_001037.4:c.265C= NP_001028.1:p.Arg89=
NM_199037.3:c.265C= NP_950238.1:p.Arg89=
XM_005259144.1:c.166C= XP_005259201.1:p.Arg56=
NM_001321605.1:c.166C= NP_001308534.1:p.Arg56=
NM_199037.4:c.265C= NP_950238.1:p.Arg89=
NM_001037.5:c.265C= MANE Select NP_001028.1:p.Arg89=
NM_001321605.2:c.166C= NP_001308534.1:p.Arg56=
NM_199037.5:c.265C= NP_950238.1:p.Arg89=