Canonical Allele Identifier: CA690167167

Gene: RPS26

Linked Data

• dbSNP Id: rs1421378881
• gnomAD v3: 12-56041587-T-G
• gnomAD v4: 12-56041587-T-G
• MyVariant Identifiers: chr12:g.56435371T>G (hg19) ; chr12:g.56041587T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56041587T>G , CM000674.2:g.56041587T>G	GRCh38
NC_000012.11:g.56435371T>G , CM000674.1:g.56435371T>G	GRCh37
NC_000012.10:g.54721638T>G	NCBI36
NG_023201.1:g.4686T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-357+191T>G	ENSP00000348849.5:n.-357+191T>G
XR_944989.1:n.126A>C
XR_944990.1:n.126A>C
XR_944989.3:n.417A>C
XR_944990.3:n.417A>C