Canonical Allele Identifier: CA690167173

Gene: RPS26

Linked Data

• dbSNP Id: rs1309853570
• gnomAD v3: 12-56041620-C-T
• gnomAD v4: 12-56041620-C-T
• MyVariant Identifiers: chr12:g.56435404C>T (hg19) ; chr12:g.56041620C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56041620C>T , CM000674.2:g.56041620C>T	GRCh38
NC_000012.11:g.56435404C>T , CM000674.1:g.56435404C>T	GRCh37
NC_000012.10:g.54721671C>T	NCBI36
NG_023201.1:g.4719C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-356-191C>T	ENSP00000348849.5:n.-356-191C>T
XR_944989.1:n.93G>A
XR_944990.1:n.93G>A
XR_944989.3:n.384G>A
XR_944990.3:n.384G>A