Canonical Allele Identifier: CA2038228914
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1895880144

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041582C>T , CM000674.2:g.56041582C>T GRCh38
NC_000012.11:g.56435366C>T , CM000674.1:g.56435366C>T GRCh37
NC_000012.10:g.54721633C>T NCBI36
NG_023201.1:g.4681C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+186C>T ENSP00000348849.5:n.-357+186C>T
XR_944989.1:n.131G>A
XR_944990.1:n.131G>A
XR_944989.3:n.422G>A
XR_944990.3:n.422G>A