Canonical Allele Identifier: CA400615046
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 2135748
ClinVar RCV Id: RCV003059718
dbSNP Id: rs1414517272
gnomAD v2: 17-62018888-G-A
MyVariant Identifiers: chr17:g.62018888G>A (hg19) chr17:g.63941528G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63941528G>A , CM000679.2:g.63941528G>A GRCh38
NC_000017.10:g.62018888G>A , CM000679.1:g.62018888G>A GRCh37
NC_000017.9:g.59372620G>A NCBI36
NG_011699.1:g.36391C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.4754C>T MANE Select ENSP00000396320.1:p.Ser1585Phe
ENST00000578147.5:c.4754C>T ENSP00000463963.1:p.Ser1585Phe
NM_000334.4:c.4754C>T MANE Select NP_000325.4:p.Ser1585Phe
XM_005257566.3:c.4754C>T XP_005257623.1:p.Ser1585Phe
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