Canonical Allele Identifier: CA947972661
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs983648187
gnomAD v3: 12-56041860-G-A
gnomAD v4: 12-56041860-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041860G>A , CM000674.2:g.56041860G>A GRCh38
NC_000012.11:g.56435644G>A , CM000674.1:g.56435644G>A GRCh37
NC_000012.10:g.54721911G>A NCBI36
NG_023201.1:g.4959G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-307G>A ENSP00000348849.5:n.-307G>A
ENST00000356464.9:c.-307G>A ENSP00000348849.5:n.-307G>A
XR_944989.3:n.144C>T
XR_944990.3:n.144C>T
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