Canonical Allele Identifier: CA304979755
Gene: ELAVL1 HGNC NCBI

Linked Data

dbSNP Id: rs569929034
gnomAD v2: 19-8469329-C-T
gnomAD v3: 19-8404445-C-T
gnomAD v4: 19-8404445-C-T
MyVariant Identifiers: chr19:g.8469329C>T (hg19) chr19:g.8404445C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8404445C>T , CM000681.2:g.8404445C>T GRCh38
NC_000019.9:g.8469329C>T , CM000681.1:g.8469329C>T GRCh37
NC_000019.8:g.8375329C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000351593.9:c.-88+40561G>A ENSP00000264073.6:n.-88+40561G>A
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