Canonical Allele Identifier: CA690167278

Gene: RPS26

Linked Data

• dbSNP Id: rs1422225257
• gnomAD v3: 12-56041876-G-A
• gnomAD v4: 12-56041876-G-A
• MyVariant Identifiers: chr12:g.56435660G>A (hg19) ; chr12:g.56041876G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56041876G>A , CM000674.2:g.56041876G>A	GRCh38
NC_000012.11:g.56435660G>A , CM000674.1:g.56435660G>A	GRCh37
NC_000012.10:g.54721927G>A	NCBI36
NG_023201.1:g.4975G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-291G>A	ENSP00000348849.5:n.-291G>A
ENST00000356464.9:c.-291G>A	ENSP00000348849.5:n.-291G>A
XR_944989.3:n.128C>T
XR_944990.3:n.128C>T