Canonical Allele Identifier: CA400616190
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1451612
ClinVar RCV Id: RCV002007313
dbSNP Id: rs121908544
MyVariant Identifiers: chr17:g.62019300G>C (hg19) chr17:g.63941940G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63941940G>C , CM000679.2:g.63941940G>C GRCh38
NC_000017.10:g.62019300G>C , CM000679.1:g.62019300G>C GRCh37
NC_000017.9:g.59373032G>C NCBI36
NG_011699.1:g.35979C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.4342C>G MANE Select ENSP00000396320.1:p.Arg1448Gly
ENST00000578147.5:c.4342C>G ENSP00000463963.1:p.Arg1448Gly
NM_000334.4:c.4342C>G MANE Select NP_000325.4:p.Arg1448Gly
XM_005257566.3:c.4342C>G XP_005257623.1:p.Arg1448Gly
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