Canonical Allele Identifier: CA237623522

Gene: RPS26

Linked Data

• dbSNP Id: rs971546279
• gnomAD v3: 12-56041759-C-A
• gnomAD v4: 12-56041759-C-A
• MyVariant Identifiers: chr12:g.56435543C>A (hg19) ; chr12:g.56041759C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56041759C>A , CM000674.2:g.56041759C>A	GRCh38
NC_000012.11:g.56435543C>A , CM000674.1:g.56435543C>A	GRCh37
NC_000012.10:g.54721810C>A	NCBI36
NG_023201.1:g.4858C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-356-52C>A	ENSP00000348849.5:n.-356-52C>A
XR_944989.3:n.245G>T
XR_944990.3:n.245G>T