Canonical Allele Identifier: CA1123769
Gene: RPS27 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000368567.4:c.-37C>T ENSP00000357555.4:n.-37C>T
NM_001349946.1:c.-254C>T NP_001336875.1:n.-254C>T
NM_001349947.1:c.-365C>T NP_001336876.1:n.-365C>T
Search 100 bp 5'
Search 100 bp 3'