Canonical Allele Identifier: CA605259067

Gene: RPS26

Linked Data

• dbSNP Id: rs1283211636
• gnomAD v2: 12-56435350-A-G
• gnomAD v3: 12-56041566-A-G
• gnomAD v4: 12-56041566-A-G
• MyVariant Identifiers: chr12:g.56435350A>G (hg19) ; chr12:g.56041566A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56041566A>G , CM000674.2:g.56041566A>G	GRCh38
NC_000012.11:g.56435350A>G , CM000674.1:g.56435350A>G	GRCh37
NC_000012.10:g.54721617A>G	NCBI36
NG_023201.1:g.4665A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-357+170A>G	ENSP00000348849.5:n.-357+170A>G
XR_944989.1:n.147T>C
XR_944990.1:n.147T>C
XR_944989.3:n.438T>C
XR_944990.3:n.438T>C