Canonical Allele Identifier: CA480184358
Gene: RPS26 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.56435458G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041674G>A , CM000674.2:g.56041674G>A GRCh38
NC_000012.11:g.56435458G>A , CM000674.1:g.56435458G>A GRCh37
NC_000012.10:g.54721725G>A NCBI36
NG_023201.1:g.4773G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-137G>A ENSP00000348849.5:n.-356-137G>A
XR_944989.1:n.39C>T
XR_944990.1:n.39C>T
XR_944989.3:n.330C>T
XR_944990.3:n.330C>T