Canonical Allele Identifier: CA501214806
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 855417
ClinVar RCV Id: RCV001060684
dbSNP Id: rs1908587559
gnomAD v3: 17-63942848-C-T
gnomAD v4: 17-63942848-C-T
MyVariant Identifiers: chr17:g.62020208C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63942848C>T , CM000679.2:g.63942848C>T GRCh38
NC_000017.10:g.62020208C>T , CM000679.1:g.62020208C>T GRCh37
NC_000017.9:g.59373940C>T NCBI36
NG_011699.1:g.35071G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.4266G>A MANE Select ENSP00000396320.1:p.Val1422=
ENST00000578147.5:c.4266G>A ENSP00000463963.1:p.Val1422=
NM_000334.4:c.4266G>A MANE Select NP_000325.4:p.Val1422=
XM_005257566.3:c.4266G>A XP_005257623.1:p.Val1422=
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