Canonical Allele Identifier: CA2586220339

Gene: RPL18

Linked Data

• ClinVar Variation Id: 2796542
• ClinVar RCV Id: RCV003670659
• gnomAD v4: 19-48616211-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48616211G>A , CM000681.2:g.48616211G>A	GRCh38
NC_000019.9:g.49119468G>A , CM000681.1:g.49119468G>A	GRCh37
NC_000019.8:g.53811280G>A	NCBI36
NG_029867.1:g.1921G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000549920.6:c.298-9C>T MANE Select	ENSP00000447001.1:n.298-9C>T
ENST00000084795.9:c.302-9C>T
ENST00000546623.5:c.224C>T
ENST00000547892.1:n.2965C>T
ENST00000547897.5:c.297+515C>T	ENSP00000470988.1:n.297+515C>T
ENST00000549273.5:c.298-9C>T	ENSP00000449610.1:n.298-9C>T
ENST00000549370.5:c.*35-9C>T	ENSP00000449067.1:n.*35-9C>T
ENST00000549533.1:n.215C>T
ENST00000549920.5:c.298-9C>T	ENSP00000447001.1:n.298-9C>T
ENST00000550645.5:c.298-306C>T	ENSP00000448899.1:n.298-306C>T
ENST00000550973.5:c.142-9C>T	ENSP00000447894.1:n.142-9C>T
ENST00000551749.5:n.1343C>T
ENST00000552347.5:n.1323C>T
ENST00000552588.5:c.211-9C>T	ENSP00000449204.1:n.211-9C>T
ENST00000552705.5:n.852C>T
NM_000979.3:c.298-9C>T	NP_000970.1:n.298-9C>T
NM_001270490.1:c.211-9C>T	NP_001257419.1:n.211-9C>T
NR_073022.1:n.565-9C>T
NM_000979.4:c.298-9C>T MANE Select	NP_000970.1:n.298-9C>T
NM_001270490.2:c.211-9C>T	NP_001257419.1:n.211-9C>T
NR_073022.2:n.325-9C>T