Canonical Allele Identifier: CA2619258077
Gene: RPS26 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041592C>G , CM000674.2:g.56041592C>G GRCh38
NC_000012.11:g.56435376C>G , CM000674.1:g.56435376C>G GRCh37
NC_000012.10:g.54721643C>G NCBI36
NG_023201.1:g.4691C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+196C>G ENSP00000348849.5:n.-357+196C>G
XR_944989.1:n.121G>C
XR_944990.1:n.121G>C
XR_944989.3:n.412G>C
XR_944990.3:n.412G>C