Canonical Allele Identifier: CA1007868451
Gene: RPS27 HGNC NCBI

Linked Data

dbSNP Id: rs758774553
gnomAD v3: 1-153991106-C-A
gnomAD v4: 1-153991106-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153991106C>A , CM000663.2:g.153991106C>A GRCh38
NC_000001.10:g.153963582C>A , CM000663.1:g.153963582C>A GRCh37
NC_000001.9:g.152230206C>A NCBI36
NG_053102.2:g.5352C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000477151.2:n.186C>A
ENST00000643794.1:c.128-9C>A ENSP00000495765.1:n.128-9C>A
ENST00000651669.1:c.7-9C>A MANE Select ENSP00000499044.1:n.7-9C>A
ENST00000368567.4:c.7-9C>A ENSP00000357555.4:n.7-9C>A
ENST00000392558.4:c.7-9C>A ENSP00000376341.4:n.7-9C>A
ENST00000477151.1:n.162-9C>A
ENST00000493224.5:n.273-9C>A
NM_001030.4:c.7-9C>A NP_001021.1:n.7-9C>A
NM_001030.6:c.7-9C>A MANE Select NP_001021.1:n.7-9C>A
NM_001349946.1:c.-90-9C>A NP_001336875.1:n.-90-9C>A
NM_001349947.1:c.-90-9C>A NP_001336876.1:n.-90-9C>A
NM_001349946.2:c.-90-9C>A NP_001336875.1:n.-90-9C>A
NM_001349947.2:c.-90-9C>A NP_001336876.1:n.-90-9C>A
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