Canonical Allele Identifier: CA690167154
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1364497936
gnomAD v3: 12-56041531-G-A
gnomAD v4: 12-56041531-G-A
MyVariant Identifiers: chr12:g.56435315G>A (hg19) chr12:g.56041531G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041531G>A , CM000674.2:g.56041531G>A GRCh38
NC_000012.11:g.56435315G>A , CM000674.1:g.56435315G>A GRCh37
NC_000012.10:g.54721582G>A NCBI36
NG_023201.1:g.4630G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+135G>A ENSP00000348849.5:n.-357+135G>A
XR_944989.1:n.182C>T
XR_944990.1:n.182C>T
XR_944989.3:n.473C>T
XR_944990.3:n.473C>T
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