Canonical Allele Identifier: CA304994980
Gene: ELAVL1 HGNC NCBI
RAB11B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs150212355
gnomAD v2: 19-8442133-G-A
gnomAD v3: 19-8377249-G-A
gnomAD v4: 19-8377249-G-A
MyVariant Identifiers: chr19:g.8442133G>A (hg19) chr19:g.8377249G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8377249G>A , CM000681.2:g.8377249G>A GRCh38
NC_000019.9:g.8442133G>A , CM000681.1:g.8442133G>A GRCh37
NC_000019.8:g.8348133G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000351593.9:c.-88+67757C>T (ELAVL1) ENSP00000264073.6:n.-88+67757C>T
NR_038237.1:n.684-182C>T (RAB11B-AS1)
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