Canonical Allele Identifier: CA884317191
Gene: ELAVL1 HGNC NCBI

Linked Data

dbSNP Id: rs1390264171
MyVariant Identifiers: chr19:g.8469514_8469515insGC (hg19) chr19:g.8404630_8404631insGC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8404630_8404631insGC , CM000681.2:g.8404630_8404631insGC GRCh38
NC_000019.9:g.8469514_8469515insGC , CM000681.1:g.8469514_8469515insGC GRCh37
NC_000019.8:g.8375514_8375515insGC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000351593.9:c.-88+40375_-88+40376insGC ENSP00000264073.6:n.-88+40375_-88+40376insGC
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