Canonical Allele Identifier: CA480184348
Gene: RPS26 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.56435454T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041670T>A , CM000674.2:g.56041670T>A GRCh38
NC_000012.11:g.56435454T>A , CM000674.1:g.56435454T>A GRCh37
NC_000012.10:g.54721721T>A NCBI36
NG_023201.1:g.4769T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-141T>A ENSP00000348849.5:n.-356-141T>A
XR_944989.1:n.43A>T
XR_944990.1:n.43A>T
XR_944989.3:n.334A>T
XR_944990.3:n.334A>T