Canonical Allele Identifier: CA6621639
Gene: RPS26 HGNC NCBI

Linked Data

dbSNP Id: rs760630234
ExAC: 12:56435939 C / T
gnomAD v2: 12-56435939-C-T
gnomAD v3: 12-56042155-C-T
gnomAD v4: 12-56042155-C-T
MyVariant Identifiers: chr12:g.56435939C>T (hg19) chr12:g.56042155C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56042155C>T , CM000674.2:g.56042155C>T GRCh38
NC_000012.11:g.56435939C>T , CM000674.1:g.56435939C>T GRCh37
NC_000012.10:g.54722206C>T NCBI36
NG_023201.1:g.5254C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356464.10:c.-12C>T ENSP00000348849.5:n.-12C>T
ENST00000646449.2:c.-12C>T MANE Select ENSP00000496643.1:n.-12C>T
ENST00000356464.9:c.-12C>T ENSP00000348849.5:n.-12C>T
ENST00000548590.1:n.16C>T
ENST00000552361.1:c.-12C>T ENSP00000450339.1:n.-12C>T
NM_001029.3:c.-12C>T NP_001020.2:n.-12C>T
NM_001029.5:c.-12C>T MANE Select NP_001020.2:n.-12C>T
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