Canonical Allele Identifier: CA480184491
Gene: RPS26 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.56435506A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041722A>C , CM000674.2:g.56041722A>C GRCh38
NC_000012.11:g.56435506A>C , CM000674.1:g.56435506A>C GRCh37
NC_000012.10:g.54721773A>C NCBI36
NG_023201.1:g.4821A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-89A>C ENSP00000348849.5:n.-356-89A>C
XR_944989.3:n.282T>G
XR_944990.3:n.282T>G