Canonical Allele Identifier: CA884315431
Gene: ELAVL1 HGNC NCBI
RAB11B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1171221667
gnomAD v3: 19-8377186-GTTAAT-G
gnomAD v4: 19-8377186-GTTAAT-G
MyVariant Identifiers: chr19:g.8442071_8442075del (hg19) chr19:g.8377187_8377191del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8377189_8377193del , CM000681.2:g.8377189_8377193del GRCh38
NC_000019.9:g.8442073_8442077del , CM000681.1:g.8442073_8442077del GRCh37
NC_000019.8:g.8348073_8348077del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000351593.9:c.-88+67815_-88+67819del (ELAVL1) ENSP00000264073.6:n.-88+67815_-88+67819del
NR_038237.1:n.684-124_684-120del (RAB11B-AS1)
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