Canonical Allele Identifier: CA690167275
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs1195791007
gnomAD v3: 12-56041875-C-T
gnomAD v4: 12-56041875-C-T
MyVariant Identifiers: chr12:g.56435659C>T (hg19) chr12:g.56041875C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56041875C>T , CM000674.2:g.56041875C>T GRCh38
NC_000012.11:g.56435659C>T , CM000674.1:g.56435659C>T GRCh37
NC_000012.10:g.54721926C>T NCBI36
NG_023201.1:g.4974C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-292C>T ENSP00000348849.5:n.-292C>T
ENST00000356464.9:c.-292C>T ENSP00000348849.5:n.-292C>T
XR_944989.3:n.129G>A
XR_944990.3:n.129G>A
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