Canonical Allele Identifier: CA2573910885
Gene: RPS27 HGNC NCBI

Linked Data

gnomAD v4: 1-153990755-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153990755T>C , CM000663.2:g.153990755T>C GRCh38
NC_000001.10:g.153963231T>C , CM000663.1:g.153963231T>C GRCh37
NC_000001.9:g.152229855T>C NCBI36
NG_053102.2:g.5001T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001349946.1:c.-259T>C NP_001336875.1:n.-259T>C
NM_001349947.1:c.-370T>C NP_001336876.1:n.-370T>C
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