Canonical Allele Identifier: CA2619258096
Gene: RPS26 HGNC NCBI

Linked Data

gnomAD v4: 12-56041600-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041600T>A , CM000674.2:g.56041600T>A GRCh38
NC_000012.11:g.56435384T>A , CM000674.1:g.56435384T>A GRCh37
NC_000012.10:g.54721651T>A NCBI36
NG_023201.1:g.4699T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+204T>A ENSP00000348849.5:n.-357+204T>A
XR_944989.1:n.113A>T
XR_944990.1:n.113A>T
XR_944989.3:n.404A>T
XR_944990.3:n.404A>T
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