Canonical Allele Identifier: CA480184234
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1295315183
gnomAD v3: 12-56041631-G-C
gnomAD v4: 12-56041631-G-C
MyVariant Identifiers: chr12:g.56435415G>C (hg19) chr12:g.56041631G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041631G>C , CM000674.2:g.56041631G>C GRCh38
NC_000012.11:g.56435415G>C , CM000674.1:g.56435415G>C GRCh37
NC_000012.10:g.54721682G>C NCBI36
NG_023201.1:g.4730G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-180G>C ENSP00000348849.5:n.-356-180G>C
XR_944989.1:n.82C>G
XR_944990.1:n.82C>G
XR_944989.3:n.373C>G
XR_944990.3:n.373C>G
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