Canonical Allele Identifier: CA2573910905
Gene: RPS27 HGNC NCBI

Linked Data

gnomAD v4: 1-153990759-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153990759G>T , CM000663.2:g.153990759G>T GRCh38
NC_000001.10:g.153963235G>T , CM000663.1:g.153963235G>T GRCh37
NC_000001.9:g.152229859G>T NCBI36
NG_053102.2:g.5005G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000368567.4:c.-38G>T ENSP00000357555.4:n.-38G>T
NM_001349946.1:c.-255G>T NP_001336875.1:n.-255G>T
NM_001349947.1:c.-366G>T NP_001336876.1:n.-366G>T
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