Canonical Allele Identifier: CA774008779
Gene: SCN4A HGNC NCBI

Linked Data

dbSNP Id: rs1311483622
MyVariant Identifiers: chr17:g.62049903C>G (hg19) chr17:g.63972543C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63972543C>G , CM000679.2:g.63972543C>G GRCh38
NC_000017.10:g.62049903C>G , CM000679.1:g.62049903C>G GRCh37
NC_000017.9:g.59403635C>G NCBI36
NG_011699.1:g.5376G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000435607.3:c.273+26G>C MANE Select ENSP00000396320.1:n.273+26G>C
ENST00000578147.5:c.273+26G>C ENSP00000463963.1:n.273+26G>C
NM_000334.4:c.273+26G>C MANE Select NP_000325.4:n.273+26G>C
XM_005257566.3:c.273+26G>C XP_005257623.1:n.273+26G>C
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