Canonical Allele Identifier: CA2038229273

Gene: RPS26

Linked Data

• dbSNP Id: rs1895886287
• gnomAD v4: 12-56041863-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56041863C>T , CM000674.2:g.56041863C>T	GRCh38
NC_000012.11:g.56435647C>T , CM000674.1:g.56435647C>T	GRCh37
NC_000012.10:g.54721914C>T	NCBI36
NG_023201.1:g.4962C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356464.10:c.-304C>T	ENSP00000348849.5:n.-304C>T
ENST00000356464.9:c.-304C>T	ENSP00000348849.5:n.-304C>T
XR_944989.3:n.141G>A
XR_944990.3:n.141G>A