Canonical Allele Identifier: CA237623419
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs887755633
gnomAD v3: 12-56041598-C-A
gnomAD v4: 12-56041598-C-A
MyVariant Identifiers: chr12:g.56435382C>A (hg19) chr12:g.56041598C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041598C>A , CM000674.2:g.56041598C>A GRCh38
NC_000012.11:g.56435382C>A , CM000674.1:g.56435382C>A GRCh37
NC_000012.10:g.54721649C>A NCBI36
NG_023201.1:g.4697C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+202C>A ENSP00000348849.5:n.-357+202C>A
XR_944989.1:n.115G>T
XR_944990.1:n.115G>T
XR_944989.3:n.406G>T
XR_944990.3:n.406G>T
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