Canonical Allele Identifier: CA400639050
Gene: SCN4A HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.62049134T>A (hg19) chr17:g.63971774T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63971774T>A , CM000679.2:g.63971774T>A GRCh38
NC_000017.10:g.62049134T>A , CM000679.1:g.62049134T>A GRCh37
NC_000017.9:g.59402866T>A NCBI36
NG_011699.1:g.6145A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.559A>T MANE Select ENSP00000396320.1:p.Thr187Ser
ENST00000578147.5:c.559A>T ENSP00000463963.1:p.Thr187Ser
NM_000334.4:c.559A>T MANE Select NP_000325.4:p.Thr187Ser
XM_005257566.3:c.559A>T XP_005257623.1:p.Thr187Ser
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