Canonical Allele Identifier: CA884315510
Gene: ELAVL1 HGNC NCBI
RAB11B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1466100219
gnomAD v3: 19-8377228-CTG-C
gnomAD v4: 19-8377228-CTG-C
MyVariant Identifiers: chr19:g.8442113_8442114del (hg19) chr19:g.8377229_8377230del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8377230_8377231del , CM000681.2:g.8377230_8377231del GRCh38
NC_000019.9:g.8442114_8442115del , CM000681.1:g.8442114_8442115del GRCh37
NC_000019.8:g.8348114_8348115del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000351593.9:c.-88+67776_-88+67777del (ELAVL1) ENSP00000264073.6:n.-88+67776_-88+67777del
NR_038237.1:n.684-163_684-162del (RAB11B-AS1)
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