Canonical Allele Identifier: CA304994993
Gene: ELAVL1 HGNC NCBI
RAB11B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs767372498
gnomAD v2: 19-8442158-A-G
gnomAD v3: 19-8377274-A-G
gnomAD v4: 19-8377274-A-G
MyVariant Identifiers: chr19:g.8442158A>G (hg19) chr19:g.8377274A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8377274A>G , CM000681.2:g.8377274A>G GRCh38
NC_000019.9:g.8442158A>G , CM000681.1:g.8442158A>G GRCh37
NC_000019.8:g.8348158A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000351593.9:c.-88+67732T>C (ELAVL1) ENSP00000264073.6:n.-88+67732T>C
NR_038237.1:n.684-207T>C (RAB11B-AS1)
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