Canonical Allele Identifier: CA1123770
Gene: RPS27 HGNC NCBI

Linked Data

dbSNP Id: rs151191078
ExAC: 1:153963236 C / G
gnomAD v2: 1-153963236-C-G
gnomAD v3: 1-153990760-C-G
gnomAD v4: 1-153990760-C-G
MyVariant Identifiers: chr1:g.153963236C>G (hg19) chr1:g.153990760C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153990760C>G , CM000663.2:g.153990760C>G GRCh38
NC_000001.10:g.153963236C>G , CM000663.1:g.153963236C>G GRCh37
NC_000001.9:g.152229860C>G NCBI36
NG_053102.2:g.5006C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368567.4:c.-37C>G ENSP00000357555.4:n.-37C>G
NM_001349946.1:c.-254C>G NP_001336875.1:n.-254C>G
NM_001349947.1:c.-365C>G NP_001336876.1:n.-365C>G
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