Canonical Allele Identifier: CA382777641

Gene: SCN4B

Linked Data

• MyVariant Identifiers: chr11:g.118012040C>A (hg19) ; chr11:g.118141325C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141325C>A , CM000673.2:g.118141325C>A	GRCh38
NC_000011.9:g.118012040C>A , CM000673.1:g.118012040C>A	GRCh37
NC_000011.8:g.117517250C>A	NCBI36
NG_011710.1:g.16591G>T , LRG_330:g.16591G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000324727.9:c.475G>T MANE Select	ENSP00000322460.4:p.Asp159Tyr
ENST00000324727.8:c.475G>T	ENSP00000322460.4:p.Asp159Tyr
ENST00000415030.6:n.618G>T
ENST00000423160.2:n.109G>T
ENST00000529878.1:c.73G>T	ENSP00000436343.1:p.Asp25Tyr
ENST00000531550.1:n.540G>T
ENST00000532138.1:n.731G>T
NM_001142348.1:c.73G>T	NP_001135820.1:p.Asp25Tyr
NM_001142349.1:c.145G>T	NP_001135821.1:p.Asp49Tyr
NM_174934.3:c.475G>T , LRG_330t1:c.475G>T	NP_777594.1:p.Asp159Tyr
NR_024527.1:n.500G>T
NM_001142348.2:c.73G>T	NP_001135820.1:p.Asp25Tyr
NM_001142349.2:c.145G>T	NP_001135821.1:p.Asp49Tyr
NR_024527.2:n.464G>T
NM_174934.4:c.475G>T MANE Select	NP_777594.1:p.Asp159Tyr