Canonical Allele Identifier: CA631359811
Gene: ELAVL1 HGNC NCBI
RAB11B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1247584494
gnomAD v2: 19-8442109-ACT-A
gnomAD v3: 19-8377225-ACT-A
gnomAD v4: 19-8377225-ACT-A
MyVariant Identifiers: chr19:g.8442110_8442111del (hg19) chr19:g.8377226_8377227del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8377228_8377229del , CM000681.2:g.8377228_8377229del GRCh38
NC_000019.9:g.8442112_8442113del , CM000681.1:g.8442112_8442113del GRCh37
NC_000019.8:g.8348112_8348113del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000351593.9:c.-88+67779_-88+67780del (ELAVL1) ENSP00000264073.6:n.-88+67779_-88+67780del
NR_038237.1:n.684-160_684-159del (RAB11B-AS1)
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