Canonical Allele Identifier: CA237623585

Gene: RPS26

Linked Data

• dbSNP Id: rs537911458
• gnomAD v2: 12-56435650-A-C
• gnomAD v3: 12-56041866-A-C
• gnomAD v4: 12-56041866-A-C
• MyVariant Identifiers: chr12:g.56435650A>C (hg19) ; chr12:g.56041866A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56041866A>C , CM000674.2:g.56041866A>C	GRCh38
NC_000012.11:g.56435650A>C , CM000674.1:g.56435650A>C	GRCh37
NC_000012.10:g.54721917A>C	NCBI36
NG_023201.1:g.4965A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-301A>C	ENSP00000348849.5:n.-301A>C
ENST00000356464.9:c.-301A>C	ENSP00000348849.5:n.-301A>C
XR_944989.3:n.138T>G
XR_944990.3:n.138T>G