Canonical Allele Identifier: CA382777640

Gene: SCN4B

Linked Data

• MyVariant Identifiers: chr11:g.118012039T>C (hg19) ; chr11:g.118141324T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118141324T>C , CM000673.2:g.118141324T>C	GRCh38
NC_000011.9:g.118012039T>C , CM000673.1:g.118012039T>C	GRCh37
NC_000011.8:g.117517249T>C	NCBI36
NG_011710.1:g.16592A>G , LRG_330:g.16592A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000324727.9:c.476A>G MANE Select	ENSP00000322460.4:p.Asp159Gly
ENST00000324727.8:c.476A>G	ENSP00000322460.4:p.Asp159Gly
ENST00000415030.6:n.619A>G
ENST00000423160.2:n.110A>G
ENST00000529878.1:c.74A>G	ENSP00000436343.1:p.Asp25Gly
ENST00000531550.1:n.541A>G
ENST00000532138.1:n.732A>G
NM_001142348.1:c.74A>G	NP_001135820.1:p.Asp25Gly
NM_001142349.1:c.146A>G	NP_001135821.1:p.Asp49Gly
NM_174934.3:c.476A>G , LRG_330t1:c.476A>G	NP_777594.1:p.Asp159Gly
NR_024527.1:n.501A>G
NM_001142348.2:c.74A>G	NP_001135820.1:p.Asp25Gly
NM_001142349.2:c.146A>G	NP_001135821.1:p.Asp49Gly
NR_024527.2:n.465A>G
NM_174934.4:c.476A>G MANE Select	NP_777594.1:p.Asp159Gly