Canonical Allele Identifier: CA480184221
Gene: RPS26 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.56435410T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041626T>G , CM000674.2:g.56041626T>G GRCh38
NC_000012.11:g.56435410T>G , CM000674.1:g.56435410T>G GRCh37
NC_000012.10:g.54721677T>G NCBI36
NG_023201.1:g.4725T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-185T>G ENSP00000348849.5:n.-356-185T>G
XR_944989.1:n.87A>C
XR_944990.1:n.87A>C
XR_944989.3:n.378A>C
XR_944990.3:n.378A>C
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