Canonical Allele Identifier: CA2648113828
Gene: RPS27 HGNC NCBI

Linked Data

gnomAD v4: 1-153990756-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153990756T>G , CM000663.2:g.153990756T>G GRCh38
NC_000001.10:g.153963232T>G , CM000663.1:g.153963232T>G GRCh37
NC_000001.9:g.152229856T>G NCBI36
NG_053102.2:g.5002T>G

Transcript Alleles

HGVS Amino-acid Change
NM_001349946.1:c.-258T>G NP_001336875.1:n.-258T>G
NM_001349947.1:c.-369T>G NP_001336876.1:n.-369T>G
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