Canonical Allele Identifier: CA690167219
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1420319573
gnomAD v3: 12-56041721-G-GA
gnomAD v4: 12-56041721-G-GA
MyVariant Identifiers: chr12:g.56435505_56435506insA (hg19) chr12:g.56041721_56041722insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041722dup , CM000674.2:g.56041722dup GRCh38
NC_000012.11:g.56435506dup , CM000674.1:g.56435506dup GRCh37
NC_000012.10:g.54721773dup NCBI36
NG_023201.1:g.4821dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-89dup ENSP00000348849.5:n.-356-89dup
XR_944989.3:n.282dup
XR_944990.3:n.282dup
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