Canonical Allele Identifier: CA501348652
Gene: SCN4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1946105
ClinVar RCV Id: RCV002667561
MyVariant Identifiers: chr17:g.62022831G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63945471G>A , CM000679.2:g.63945471G>A GRCh38
NC_000017.10:g.62022831G>A , CM000679.1:g.62022831G>A GRCh37
NC_000017.9:g.59376563G>A NCBI36
NG_011699.1:g.32448C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.3609C>T MANE Select ENSP00000396320.1:p.Val1203=
ENST00000578147.5:c.3609C>T ENSP00000463963.1:p.Val1203=
NM_000334.4:c.3609C>T MANE Select NP_000325.4:p.Val1203=
XM_005257566.3:c.3609C>T XP_005257623.1:p.Val1203=
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