Canonical Allele Identifier: CA690167290
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs937888249
gnomAD v3: 12-56041905-G-T
gnomAD v4: 12-56041905-G-T
MyVariant Identifiers: chr12:g.56435689G>T (hg19) chr12:g.56041905G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041905G>T , CM000674.2:g.56041905G>T GRCh38
NC_000012.11:g.56435689G>T , CM000674.1:g.56435689G>T GRCh37
NC_000012.10:g.54721956G>T NCBI36
NG_023201.1:g.5004G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-262G>T ENSP00000348849.5:n.-262G>T
ENST00000356464.9:c.-262G>T ENSP00000348849.5:n.-262G>T
ENST00000552361.1:c.-194G>T ENSP00000450339.1:n.-194G>T
NM_001029.3:c.-262G>T NP_001020.2:n.-262G>T
XR_944989.3:n.99C>A
XR_944990.3:n.99C>A
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