Canonical Allele Identifier: CA631359802
Gene: ELAVL1 HGNC NCBI
RAB11B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs572716923
gnomAD v2: 19-8442074-A-ATT
gnomAD v3: 19-8377190-A-ATT
gnomAD v4: 19-8377190-A-ATT
MyVariant Identifiers: chr19:g.8442077_8442078insTT (hg19) chr19:g.8442074_8442075insTT (hg19) chr19:g.8377193_8377194insTT (hg38) chr19:g.8377190_8377191insTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.8377207_8377208dup , CM000681.2:g.8377207_8377208dup GRCh38
NC_000019.9:g.8442091_8442092dup , CM000681.1:g.8442091_8442092dup GRCh37
NC_000019.8:g.8348091_8348092dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000351593.9:c.-88+67814_-88+67815dup (ELAVL1) ENSP00000264073.6:n.-88+67814_-88+67815dup
NR_038237.1:n.684-125_684-124dup (RAB11B-AS1)
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