Canonical Allele Identifier: CA889550303
Gene: RPS27 HGNC NCBI

Linked Data

dbSNP Id: rs773902654
gnomAD v3: 1-153990761-T-C
gnomAD v4: 1-153990761-T-C
MyVariant Identifiers: chr1:g.153963237T>C (hg19) chr1:g.153990761T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153990761T>C , CM000663.2:g.153990761T>C GRCh38
NC_000001.10:g.153963237T>C , CM000663.1:g.153963237T>C GRCh37
NC_000001.9:g.152229861T>C NCBI36
NG_053102.2:g.5007T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368567.4:c.-36T>C ENSP00000357555.4:n.-36T>C
NM_001349946.1:c.-253T>C NP_001336875.1:n.-253T>C
NM_001349947.1:c.-364T>C NP_001336876.1:n.-364T>C
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