Canonical Allele Identifier: CA480184233
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1295315183
MyVariant Identifiers: chr12:g.56435415G>A (hg19)
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Genomic Alleles

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

Transcript Alleles

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