Canonical Allele Identifier: CA304994964
Gene: ELAVL1 HGNC NCBI
RAB11B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs900811936
gnomAD v2: 19-8442078-T-C
gnomAD v3: 19-8377194-T-C
gnomAD v4: 19-8377194-T-C
MyVariant Identifiers: chr19:g.8442078T>C (hg19) chr19:g.8377194T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8377194T>C , CM000681.2:g.8377194T>C GRCh38
NC_000019.9:g.8442078T>C , CM000681.1:g.8442078T>C GRCh37
NC_000019.8:g.8348078T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000351593.9:c.-88+67812A>G (ELAVL1) ENSP00000264073.6:n.-88+67812A>G
NR_038237.1:n.684-127A>G (RAB11B-AS1)
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