Canonical Allele Identifier: CA2619258139
Gene: RPS26 HGNC NCBI

Linked Data

gnomAD v4: 12-56041615-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041615C>T , CM000674.2:g.56041615C>T GRCh38
NC_000012.11:g.56435399C>T , CM000674.1:g.56435399C>T GRCh37
NC_000012.10:g.54721666C>T NCBI36
NG_023201.1:g.4714C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-196C>T ENSP00000348849.5:n.-356-196C>T
XR_944989.1:n.98G>A
XR_944990.1:n.98G>A
XR_944989.3:n.389G>A
XR_944990.3:n.389G>A
Search 100 bp 5'
Search 100 bp 3'