Canonical Allele Identifier: CA304994968
Gene: ELAVL1 HGNC NCBI
RAB11B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs901383234
gnomAD v3: 19-8377215-CAA-C
gnomAD v4: 19-8377215-CAA-C
MyVariant Identifiers: chr19:g.8442100_8442101del (hg19) chr19:g.8377216_8377217del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8377216_8377217del , CM000681.2:g.8377216_8377217del GRCh38
NC_000019.9:g.8442100_8442101del , CM000681.1:g.8442100_8442101del GRCh37
NC_000019.8:g.8348100_8348101del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000351593.9:c.-88+67789_-88+67790del (ELAVL1) ENSP00000264073.6:n.-88+67789_-88+67790del
NR_038237.1:n.684-150_684-149del (RAB11B-AS1)
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