Canonical Allele Identifier: CA631359767
Gene: ELAVL1 HGNC NCBI
RAB11B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1225549852
gnomAD v2: 19-8441776-A-G
gnomAD v3: 19-8376892-A-G
gnomAD v4: 19-8376892-A-G
MyVariant Identifiers: chr19:g.8441776A>G (hg19) chr19:g.8376892A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8376892A>G , CM000681.2:g.8376892A>G GRCh38
NC_000019.9:g.8441776A>G , CM000681.1:g.8441776A>G GRCh37
NC_000019.8:g.8347776A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000351593.9:c.-88+68114T>C (ELAVL1) ENSP00000264073.6:n.-88+68114T>C
NR_038237.1:n.789+70T>C (RAB11B-AS1)
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