Canonical Allele Identifier: CA480184705
Gene: RPS26 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.56435581G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041797G>T , CM000674.2:g.56041797G>T GRCh38
NC_000012.11:g.56435581G>T , CM000674.1:g.56435581G>T GRCh37
NC_000012.10:g.54721848G>T NCBI36
NG_023201.1:g.4896G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-14G>T ENSP00000348849.5:n.-356-14G>T
XR_944989.3:n.207C>A
XR_944990.3:n.207C>A