Canonical Allele Identifier: CA2564022000
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041591T>G , CM000674.2:g.56041591T>G GRCh38
NC_000012.11:g.56435375T>G , CM000674.1:g.56435375T>G GRCh37
NC_000012.10:g.54721642T>G NCBI36
NG_023201.1:g.4690T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+195T>G ENSP00000348849.5:n.-357+195T>G
XR_944989.1:n.122A>C
XR_944990.1:n.122A>C
XR_944989.3:n.413A>C
XR_944990.3:n.413A>C