Canonical Allele Identifier: CA505270259
Gene: ELAVL1 HGNC NCBI
RAB11B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1971225136
gnomAD v4: 19-8376985-T-C
MyVariant Identifiers: chr19:g.8441869T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8376985T>C , CM000681.2:g.8376985T>C GRCh38
NC_000019.9:g.8441869T>C , CM000681.1:g.8441869T>C GRCh37
NC_000019.8:g.8347869T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000351593.9:c.-88+68021A>G (ELAVL1) ENSP00000264073.6:n.-88+68021A>G
NR_038237.1:n.766A>G (RAB11B-AS1)