Canonical Allele Identifier: CA237623434

Gene: RPS26

Linked Data

• dbSNP Id: rs983532901
• gnomAD v2: 12-56435449-C-G
• gnomAD v3: 12-56041665-C-G
• gnomAD v4: 12-56041665-C-G
• MyVariant Identifiers: chr12:g.56435449C>G (hg19) ; chr12:g.56041665C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56041665C>G , CM000674.2:g.56041665C>G	GRCh38
NC_000012.11:g.56435449C>G , CM000674.1:g.56435449C>G	GRCh37
NC_000012.10:g.54721716C>G	NCBI36
NG_023201.1:g.4764C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-356-146C>G	ENSP00000348849.5:n.-356-146C>G
XR_944989.1:n.48G>C
XR_944990.1:n.48G>C
XR_944989.3:n.339G>C
XR_944990.3:n.339G>C