Canonical Allele Identifier: CA505270596
Gene: ELAVL1 HGNC NCBI
RAB11B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1485104804
gnomAD v2: 19-8441975-GAAATA-G
gnomAD v3: 19-8377091-GAAATA-G
gnomAD v4: 19-8377091-GAAATA-G
MyVariant Identifiers: chr19:g.8441976_8441980del (hg19) chr19:g.8377092_8377096del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8377100_8377104del , CM000681.2:g.8377100_8377104del GRCh38
NC_000019.9:g.8441984_8441988del , CM000681.1:g.8441984_8441988del GRCh37
NC_000019.8:g.8347984_8347988del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000351593.9:c.-88+67910_-88+67914del (ELAVL1) ENSP00000264073.6:n.-88+67910_-88+67914del
NR_038237.1:n.684-29_684-25del (RAB11B-AS1)
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