Canonical Allele Identifier: CA2619258744
Gene: RPS26 HGNC NCBI

Linked Data

gnomAD v4: 12-56041878-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041878G>A , CM000674.2:g.56041878G>A GRCh38
NC_000012.11:g.56435662G>A , CM000674.1:g.56435662G>A GRCh37
NC_000012.10:g.54721929G>A NCBI36
NG_023201.1:g.4977G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-289G>A ENSP00000348849.5:n.-289G>A
ENST00000356464.9:c.-289G>A ENSP00000348849.5:n.-289G>A
XR_944989.3:n.126C>T
XR_944990.3:n.126C>T
Search 100 bp 5'
Search 100 bp 3'