Canonical Allele Identifier: CA405328880
Gene: SCN1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35033658G>C , CM000681.2:g.35033658G>C GRCh38
NC_000019.9:g.35524562G>C , CM000681.1:g.35524562G>C GRCh37
NC_000019.8:g.40216402G>C NCBI36
NG_013359.1:g.7971G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000415950.5:c.367G>C ENSP00000396915.2:p.Val123Leu
ENST00000262631.11:c.367G>C MANE Select ENSP00000262631.3:p.Val123Leu
ENST00000415950.4:c.367G>C ENSP00000396915.2:p.Val123Leu
ENST00000596348.2:c.268G>C ENSP00000492247.1:p.Val90Leu
ENST00000638536.1:c.367G>C ENSP00000492022.1:p.Val123Leu
ENST00000640135.1:c.268G>C ENSP00000492655.1:p.Val90Leu
ENST00000675741.1:c.268G>C ENSP00000502395.1:p.Val90Leu
ENST00000676410.1:c.268G>C ENSP00000502717.1:p.Val90Leu
ENST00000262631.9:c.367G>C ENSP00000262631.3:p.Val123Leu
ENST00000415950.3:c.367G>C ENSP00000396915.2:p.Val123Leu
ENST00000595652.5:c.208-54G>C ENSP00000468848.1:n.208-54G>C
ENST00000596348.1:n.376G>C
NM_001037.4:c.367G>C NP_001028.1:p.Val123Leu
NM_199037.3:c.367G>C NP_950238.1:p.Val123Leu
XM_005259144.1:c.268G>C XP_005259201.1:p.Val90Leu
NM_001321605.1:c.268G>C NP_001308534.1:p.Val90Leu
NM_199037.4:c.367G>C NP_950238.1:p.Val123Leu
NM_001037.5:c.367G>C MANE Select NP_001028.1:p.Val123Leu
NM_001321605.2:c.268G>C NP_001308534.1:p.Val90Leu
NM_199037.5:c.367G>C NP_950238.1:p.Val123Leu