Canonical Allele Identifier: CA237623396

Gene: RPS26

Linked Data

• dbSNP Id: rs776633677
• gnomAD v2: 12-56435336-T-C
• gnomAD v3: 12-56041552-T-C
• gnomAD v4: 12-56041552-T-C
• MyVariant Identifiers: chr12:g.56435336T>C (hg19) ; chr12:g.56041552T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56041552T>C , CM000674.2:g.56041552T>C	GRCh38
NC_000012.11:g.56435336T>C , CM000674.1:g.56435336T>C	GRCh37
NC_000012.10:g.54721603T>C	NCBI36
NG_023201.1:g.4651T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-357+156T>C	ENSP00000348849.5:n.-357+156T>C
XR_944989.1:n.161A>G
XR_944990.1:n.161A>G
XR_944989.3:n.452A>G
XR_944990.3:n.452A>G