Canonical Allele Identifier: CA480184295
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1895881223
MyVariant Identifiers: chr12:g.56435435A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041651A>G , CM000674.2:g.56041651A>G GRCh38
NC_000012.11:g.56435435A>G , CM000674.1:g.56435435A>G GRCh37
NC_000012.10:g.54721702A>G NCBI36
NG_023201.1:g.4750A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-160A>G ENSP00000348849.5:n.-356-160A>G
XR_944989.1:n.62T>C
XR_944990.1:n.62T>C
XR_944989.3:n.353T>C
XR_944990.3:n.353T>C