Canonical Allele Identifier: CA382777658

Gene: SCN4B

Linked Data

• MyVariant Identifiers: chr11:g.118012048T>A (hg19) ; chr11:g.118141333T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141333T>A , CM000673.2:g.118141333T>A	GRCh38
NC_000011.9:g.118012048T>A , CM000673.1:g.118012048T>A	GRCh37
NC_000011.8:g.117517258T>A	NCBI36
NG_011710.1:g.16583A>T , LRG_330:g.16583A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000324727.9:c.467A>T MANE Select	ENSP00000322460.4:p.Glu156Val
ENST00000324727.8:c.467A>T	ENSP00000322460.4:p.Glu156Val
ENST00000415030.6:n.610A>T
ENST00000423160.2:n.101A>T
ENST00000529878.1:c.65A>T	ENSP00000436343.1:p.Glu22Val
ENST00000531550.1:n.532A>T
ENST00000532138.1:n.723A>T
NM_001142348.1:c.65A>T	NP_001135820.1:p.Glu22Val
NM_001142349.1:c.137A>T	NP_001135821.1:p.Glu46Val
NM_174934.3:c.467A>T , LRG_330t1:c.467A>T	NP_777594.1:p.Glu156Val
NR_024527.1:n.492A>T
NM_001142348.2:c.65A>T	NP_001135820.1:p.Glu22Val
NM_001142349.2:c.137A>T	NP_001135821.1:p.Glu46Val
NR_024527.2:n.456A>T
NM_174934.4:c.467A>T MANE Select	NP_777594.1:p.Glu156Val