Canonical Allele Identifier: CA2038228855

Gene: RPS26

Linked Data

• dbSNP Id: rs1895879021

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56041515T>G , CM000674.2:g.56041515T>G	GRCh38
NC_000012.11:g.56435299T>G , CM000674.1:g.56435299T>G	GRCh37
NC_000012.10:g.54721566T>G	NCBI36
NG_023201.1:g.4614T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-357+119T>G	ENSP00000348849.5:n.-357+119T>G
XR_944989.1:n.198A>C
XR_944990.1:n.198A>C
XR_944989.3:n.489A>C
XR_944990.3:n.489A>C