Canonical Allele Identifier: CA480184457

Gene: RPS26

Linked Data

• dbSNP Id: rs147303343
• MyVariant Identifiers: chr12:g.56435494G>C (hg19) ; chr12:g.56041710G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56041710G>C , CM000674.2:g.56041710G>C	GRCh38
NC_000012.11:g.56435494G>C , CM000674.1:g.56435494G>C	GRCh37
NC_000012.10:g.54721761G>C	NCBI36
NG_023201.1:g.4809G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-356-101G>C	ENSP00000348849.5:n.-356-101G>C
XR_944989.1:n.3C>G
XR_944990.1:n.3C>G
XR_944989.3:n.294C>G
XR_944990.3:n.294C>G