Canonical Allele Identifier: CA505270380
Gene: ELAVL1 HGNC NCBI
RAB11B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1159358486
gnomAD v3: 19-8377019-G-A
gnomAD v4: 19-8377019-G-A
MyVariant Identifiers: chr19:g.8441903G>A (hg19) chr19:g.8377019G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8377019G>A , CM000681.2:g.8377019G>A GRCh38
NC_000019.9:g.8441903G>A , CM000681.1:g.8441903G>A GRCh37
NC_000019.8:g.8347903G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000351593.9:c.-88+67987C>T (ELAVL1) ENSP00000264073.6:n.-88+67987C>T
NR_038237.1:n.732C>T (RAB11B-AS1)
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