Canonical Allele Identifier: CA2038229282
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1895886453
gnomAD v4: 12-56041869-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041869T>A , CM000674.2:g.56041869T>A GRCh38
NC_000012.11:g.56435653T>A , CM000674.1:g.56435653T>A GRCh37
NC_000012.10:g.54721920T>A NCBI36
NG_023201.1:g.4968T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-298T>A ENSP00000348849.5:n.-298T>A
ENST00000356464.9:c.-298T>A ENSP00000348849.5:n.-298T>A
XR_944989.3:n.135A>T
XR_944990.3:n.135A>T
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