Canonical Allele Identifier: CA2619258102
Gene: RPS26 HGNC NCBI

Linked Data

gnomAD v4: 12-56041603-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041603C>A , CM000674.2:g.56041603C>A GRCh38
NC_000012.11:g.56435387C>A , CM000674.1:g.56435387C>A GRCh37
NC_000012.10:g.54721654C>A NCBI36
NG_023201.1:g.4702C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-208C>A ENSP00000348849.5:n.-356-208C>A
XR_944989.1:n.110G>T
XR_944990.1:n.110G>T
XR_944989.3:n.401G>T
XR_944990.3:n.401G>T
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