Canonical Allele Identifier: CA123618
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 13900
dbSNP Id: rs11554290
COSMIC: COSM584
CIViC: CA123618

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713908T>C , CM000663.2:g.114713908T>C GRCh38
NC_000001.10:g.115256529T>C , CM000663.1:g.115256529T>C GRCh37
NC_000001.9:g.115058052T>C NCBI36
NG_007572.1:g.7987A>G , LRG_92:g.7987A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.182A>G MANE Select ENSP00000358548.4:p.Gln61Arg
ENST00000369535.4:c.182A>G ENSP00000358548.4:p.Gln61Arg
NM_002524.4:c.182A>G NP_002515.1:p.Gln61Arg
NM_002524.5:c.182A>G MANE Select NP_002515.1:p.Gln61Arg