Canonical Allele Identifier: CA2038229323
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1341374793
gnomAD v4: 12-56041902-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041902G>C , CM000674.2:g.56041902G>C GRCh38
NC_000012.11:g.56435686G>C , CM000674.1:g.56435686G>C GRCh37
NC_000012.10:g.54721953G>C NCBI36
NG_023201.1:g.5001G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-265G>C ENSP00000348849.5:n.-265G>C
ENST00000356464.9:c.-265G>C ENSP00000348849.5:n.-265G>C
ENST00000552361.1:c.-197G>C ENSP00000450339.1:n.-197G>C
NM_001029.3:c.-265G>C NP_001020.2:n.-265G>C
XR_944989.3:n.102C>G
XR_944990.3:n.102C>G
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