Canonical Allele Identifier: CA16602358
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 375871
dbSNP Id: rs121913255
COSMIC: COSM586

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713907T>G , CM000663.2:g.114713907T>G GRCh38
NC_000001.10:g.115256528T>G , CM000663.1:g.115256528T>G GRCh37
NC_000001.9:g.115058051T>G NCBI36
NG_007572.1:g.7988A>C , LRG_92:g.7988A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.183A>C MANE Select ENSP00000358548.4:p.Gln61His
ENST00000369535.4:c.183A>C ENSP00000358548.4:p.Gln61His
NM_002524.4:c.183A>C NP_002515.1:p.Gln61His
NM_002524.5:c.183A>C MANE Select NP_002515.1:p.Gln61His