Canonical Allele Identifier: CA2619258082
Gene: RPS26 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041595A>T , CM000674.2:g.56041595A>T GRCh38
NC_000012.11:g.56435379A>T , CM000674.1:g.56435379A>T GRCh37
NC_000012.10:g.54721646A>T NCBI36
NG_023201.1:g.4694A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-357+199A>T ENSP00000348849.5:n.-357+199A>T
XR_944989.1:n.118T>A
XR_944990.1:n.118T>A
XR_944989.3:n.409T>A
XR_944990.3:n.409T>A