Canonical Allele Identifier: CA947972297
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1895880502
gnomAD v3: 12-56041603-C-G
gnomAD v4: 12-56041603-C-G
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Genomic Alleles

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

Transcript Alleles

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