Canonical Allele Identifier: CA237623496

Gene: RPS26

Linked Data

• dbSNP Id: rs1052808304
• gnomAD v2: 12-56435498-A-G
• gnomAD v3: 12-56041714-A-G
• gnomAD v4: 12-56041714-A-G
• MyVariant Identifiers: chr12:g.56435498A>G (hg19) ; chr12:g.56435498_56435499delinsGG (hg19) ; chr12:g.56041714A>G (hg38) ; chr12:g.56041714_56041715delinsGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56041714A>G , CM000674.2:g.56041714A>G	GRCh38
NC_000012.11:g.56435498A>G , CM000674.1:g.56435498A>G	GRCh37
NC_000012.10:g.54721765A>G	NCBI36
NG_023201.1:g.4813A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-356-97A>G	ENSP00000348849.5:n.-356-97A>G
XR_944989.3:n.290T>C
XR_944990.3:n.290T>C