Canonical Allele Identifier: CA2561972562
Gene: RPS26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041556T>C , CM000674.2:g.56041556T>C GRCh38
NC_000012.11:g.56435340T>C , CM000674.1:g.56435340T>C GRCh37
NC_000012.10:g.54721607T>C NCBI36
NG_023201.1:g.4655T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+160T>C ENSP00000348849.5:n.-357+160T>C
XR_944989.1:n.157A>G
XR_944990.1:n.157A>G
XR_944989.3:n.448A>G
XR_944990.3:n.448A>G