Canonical Allele Identifier: CA30768721

Gene: RPS27

Linked Data

• dbSNP Id: rs965272200
• MyVariant Identifiers: chr1:g.153963522T>C (hg19) ; chr1:g.153991046T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991046T>C , CM000663.2:g.153991046T>C	GRCh38
NC_000001.10:g.153963522T>C , CM000663.1:g.153963522T>C	GRCh37
NC_000001.9:g.152230146T>C	NCBI36
NG_053102.2:g.5292T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.126T>C
ENST00000643794.1:c.127+12T>C	ENSP00000495765.1:n.127+12T>C
ENST00000651669.1:c.7-69T>C MANE Select	ENSP00000499044.1:n.7-69T>C
ENST00000368567.4:c.7-69T>C	ENSP00000357555.4:n.7-69T>C
ENST00000392558.4:c.7-69T>C	ENSP00000376341.4:n.7-69T>C
ENST00000477151.1:n.161+12T>C
ENST00000493224.5:n.272+12T>C
NM_001030.4:c.7-69T>C	NP_001021.1:n.7-69T>C
NM_001030.6:c.7-69T>C MANE Select	NP_001021.1:n.7-69T>C
NM_001349946.1:c.-91+12T>C	NP_001336875.1:n.-91+12T>C
NM_001349947.1:c.-91+12T>C	NP_001336876.1:n.-91+12T>C
NM_001349946.2:c.-91+12T>C	NP_001336875.1:n.-91+12T>C
NM_001349947.2:c.-91+12T>C	NP_001336876.1:n.-91+12T>C