Canonical Allele Identifier: CA633604290
Gene: RPL18 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48615466G>T , CM000681.2:g.48615466G>T GRCh38
NC_000019.9:g.49118723G>T , CM000681.1:g.49118723G>T GRCh37
NC_000019.8:g.53810535G>T NCBI36
NG_029867.1:g.1176G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000549920.6:c.492-19C>A MANE Select ENSP00000447001.1:n.492-19C>A
ENST00000084795.9:c.496-19C>A
ENST00000546623.5:c.427-19C>A
ENST00000547892.1:n.3710C>A
ENST00000547897.5:c.298-19C>A ENSP00000470988.1:n.298-19C>A
ENST00000549273.5:c.*407C>A ENSP00000449610.1:n.*407C>A
ENST00000549370.5:c.*229-19C>A ENSP00000449067.1:n.*229-19C>A
ENST00000549533.1:n.550-19C>A
ENST00000549920.5:c.492-19C>A ENSP00000447001.1:n.492-19C>A
ENST00000550645.5:c.327-19C>A ENSP00000448899.1:n.327-19C>A
ENST00000550973.5:c.336-19C>A ENSP00000447894.1:n.336-19C>A
ENST00000551749.5:n.1956C>A
ENST00000552347.5:n.1526-19C>A
ENST00000552588.5:c.405-19C>A ENSP00000449204.1:n.405-19C>A
NM_000979.3:c.492-19C>A NP_000970.1:n.492-19C>A
NM_001270490.1:c.405-19C>A NP_001257419.1:n.405-19C>A
NR_073022.1:n.759-19C>A
NM_000979.4:c.492-19C>A MANE Select NP_000970.1:n.492-19C>A
NM_001270490.2:c.405-19C>A NP_001257419.1:n.405-19C>A
NR_073022.2:n.519-19C>A