Canonical Allele Identifier: CA304979834
Gene: ELAVL1 HGNC NCBI

Linked Data

dbSNP Id: rs557979672
MyVariant Identifiers: chr19:g.8404530C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8404530C>G , CM000681.2:g.8404530C>G GRCh38
NC_000019.9:g.8469414C>G , CM000681.1:g.8469414C>G GRCh37
NC_000019.8:g.8375414C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000351593.9:c.-88+40476G>C ENSP00000264073.6:n.-88+40476G>C
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