Canonical Allele Identifier: CA2619258762
Gene: RPS26 HGNC NCBI

Linked Data

gnomAD v4: 12-56041896-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041896T>C , CM000674.2:g.56041896T>C GRCh38
NC_000012.11:g.56435680T>C , CM000674.1:g.56435680T>C GRCh37
NC_000012.10:g.54721947T>C NCBI36
NG_023201.1:g.4995T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-271T>C ENSP00000348849.5:n.-271T>C
ENST00000356464.9:c.-271T>C ENSP00000348849.5:n.-271T>C
ENST00000552361.1:c.-203T>C ENSP00000450339.1:n.-203T>C
XR_944989.3:n.108A>G
XR_944990.3:n.108A>G
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