Canonical Allele Identifier: CA626860772
Gene: SCN4A HGNC NCBI

Linked Data

dbSNP Id: rs79250390
gnomAD v2: 17-62019656-A-T
gnomAD v3: 17-63942296-A-T
gnomAD v4: 17-63942296-A-T
MyVariant Identifiers: chr17:g.62019656A>T (hg19) chr17:g.63942296A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63942296A>T , CM000679.2:g.63942296A>T GRCh38
NC_000017.10:g.62019656A>T , CM000679.1:g.62019656A>T GRCh37
NC_000017.9:g.59373388A>T NCBI36
NG_011699.1:g.35623T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000435607.3:c.4289-303T>A MANE Select ENSP00000396320.1:n.4289-303T>A
ENST00000578147.5:c.4289-303T>A ENSP00000463963.1:n.4289-303T>A
NM_000334.4:c.4289-303T>A MANE Select NP_000325.4:n.4289-303T>A
XM_005257566.3:c.4289-303T>A XP_005257623.1:n.4289-303T>A
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