Canonical Allele Identifier: CA2619258739
Gene: RPS26 HGNC NCBI

Linked Data

gnomAD v4: 12-56041871-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041871C>A , CM000674.2:g.56041871C>A GRCh38
NC_000012.11:g.56435655C>A , CM000674.1:g.56435655C>A GRCh37
NC_000012.10:g.54721922C>A NCBI36
NG_023201.1:g.4970C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-296C>A ENSP00000348849.5:n.-296C>A
ENST00000356464.9:c.-296C>A ENSP00000348849.5:n.-296C>A
XR_944989.3:n.133G>T
XR_944990.3:n.133G>T
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