Canonical Allele Identifier: CA237623385

Gene: RPS26

Linked Data

• dbSNP Id: rs966773516
• gnomAD v2: 12-56435326-T-C
• gnomAD v3: 12-56041542-T-C
• gnomAD v4: 12-56041542-T-C
• MyVariant Identifiers: chr12:g.56435326T>C (hg19) ; chr12:g.56041542T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56041542T>C , CM000674.2:g.56041542T>C	GRCh38
NC_000012.11:g.56435326T>C , CM000674.1:g.56435326T>C	GRCh37
NC_000012.10:g.54721593T>C	NCBI36
NG_023201.1:g.4641T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-357+146T>C	ENSP00000348849.5:n.-357+146T>C
XR_944989.1:n.171A>G
XR_944990.1:n.171A>G
XR_944989.3:n.462A>G
XR_944990.3:n.462A>G