Canonical Allele Identifier: CA480184716
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1895885074
gnomAD v4: 12-56041802-G-A
MyVariant Identifiers: chr12:g.56435586G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041802G>A , CM000674.2:g.56041802G>A GRCh38
NC_000012.11:g.56435586G>A , CM000674.1:g.56435586G>A GRCh37
NC_000012.10:g.54721853G>A NCBI36
NG_023201.1:g.4901G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-356-9G>A ENSP00000348849.5:n.-356-9G>A
XR_944989.3:n.202C>T
XR_944990.3:n.202C>T
Search 100 bp 5'
Search 100 bp 3'