Canonical Allele Identifier: CA477355799

Gene: SCN4B

Linked Data

• gnomAD v4: 11-118143897-C-A
• MyVariant Identifiers: chr11:g.118014612C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118143897C>A , CM000673.2:g.118143897C>A	GRCh38
NC_000011.9:g.118014612C>A , CM000673.1:g.118014612C>A	GRCh37
NC_000011.8:g.117519822C>A	NCBI36
NG_011710.1:g.14019G>T , LRG_330:g.14019G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324727.9:c.399G>T MANE Select	ENSP00000322460.4:p.Val133=
ENST00000324727.8:c.399G>T	ENSP00000322460.4:p.Val133=
ENST00000415030.6:n.542G>T
ENST00000529878.1:c.62-2561G>T	ENSP00000436343.1:n.62-2561G>T
ENST00000532138.1:n.719+90G>T
NM_001142348.1:c.62-2561G>T	NP_001135820.1:n.62-2561G>T
NM_001142349.1:c.69G>T	NP_001135821.1:p.Val23=
NM_174934.3:c.399G>T , LRG_330t1:c.399G>T	NP_777594.1:p.Val133=
NR_024527.1:n.488+90G>T
NM_001142348.2:c.62-2561G>T	NP_001135820.1:n.62-2561G>T
NM_001142349.2:c.69G>T	NP_001135821.1:p.Val23=
NR_024527.2:n.452+90G>T
NM_174934.4:c.399G>T MANE Select	NP_777594.1:p.Val133=