Canonical Allele Identifier: CA2576840065

Gene: RPL18

Linked Data

• ClinVar Variation Id: 3030413
• ClinVar RCV Id: RCV003901614

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48617884G>A , CM000681.2:g.48617884G>A	GRCh38
NC_000019.9:g.49121141G>A , CM000681.1:g.49121141G>A	GRCh37
NC_000019.8:g.53812953G>A	NCBI36
NG_029867.1:g.3594G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000549920.6:c.4-7C>T MANE Select	ENSP00000447001.1:n.4-7C>T
ENST00000084795.9:c.1C>T
ENST00000547892.1:n.1292C>T
ENST00000547897.5:c.4-7C>T	ENSP00000470988.1:n.4-7C>T
ENST00000549273.5:c.4-7C>T	ENSP00000449610.1:n.4-7C>T
ENST00000549370.5:c.4-7C>T	ENSP00000449067.1:n.4-7C>T
ENST00000549920.5:c.4-7C>T	ENSP00000447001.1:n.4-7C>T
ENST00000550645.5:c.4-7C>T	ENSP00000448899.1:n.4-7C>T
ENST00000550671.1:n.45-7C>T
ENST00000550973.5:c.-153-7C>T	ENSP00000447894.1:n.-153-7C>T
ENST00000551749.5:n.44-7C>T
ENST00000552347.5:n.24-7C>T
ENST00000552588.5:c.4-461C>T	ENSP00000449204.1:n.4-461C>T
ENST00000552705.5:n.44-7C>T
ENST00000552851.1:n.25-461C>T
NM_000979.3:c.4-7C>T	NP_000970.1:n.4-7C>T
NM_001270490.1:c.4-461C>T	NP_001257419.1:n.4-461C>T
NR_073022.1:n.279-7C>T
NM_000979.4:c.4-7C>T MANE Select	NP_000970.1:n.4-7C>T
NM_001270490.2:c.4-461C>T	NP_001257419.1:n.4-461C>T
NR_073022.2:n.39-7C>T