Canonical Allele Identifier: CA480184329
Gene: RPS26 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.56435447C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041663C>G , CM000674.2:g.56041663C>G GRCh38
NC_000012.11:g.56435447C>G , CM000674.1:g.56435447C>G GRCh37
NC_000012.10:g.54721714C>G NCBI36
NG_023201.1:g.4762C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-148C>G ENSP00000348849.5:n.-356-148C>G
XR_944989.1:n.50G>C
XR_944990.1:n.50G>C
XR_944989.3:n.341G>C
XR_944990.3:n.341G>C