Canonical Allele Identifier: CA1007868441
Gene: RPS27 HGNC NCBI

Linked Data

dbSNP Id: rs1649370995
gnomAD v3: 1-153991105-T-C
gnomAD v4: 1-153991105-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153991105T>C , CM000663.2:g.153991105T>C GRCh38
NC_000001.10:g.153963581T>C , CM000663.1:g.153963581T>C GRCh37
NC_000001.9:g.152230205T>C NCBI36
NG_053102.2:g.5351T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000477151.2:n.185T>C
ENST00000643794.1:c.128-10T>C ENSP00000495765.1:n.128-10T>C
ENST00000651669.1:c.7-10T>C MANE Select ENSP00000499044.1:n.7-10T>C
ENST00000368567.4:c.7-10T>C ENSP00000357555.4:n.7-10T>C
ENST00000392558.4:c.7-10T>C ENSP00000376341.4:n.7-10T>C
ENST00000477151.1:n.162-10T>C
ENST00000493224.5:n.273-10T>C
NM_001030.4:c.7-10T>C NP_001021.1:n.7-10T>C
NM_001030.6:c.7-10T>C MANE Select NP_001021.1:n.7-10T>C
NM_001349946.1:c.-90-10T>C NP_001336875.1:n.-90-10T>C
NM_001349947.1:c.-90-10T>C NP_001336876.1:n.-90-10T>C
NM_001349946.2:c.-90-10T>C NP_001336875.1:n.-90-10T>C
NM_001349947.2:c.-90-10T>C NP_001336876.1:n.-90-10T>C
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