Canonical Allele Identifier: CA341741583
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 933172
ClinVar RCV Id: RCV001201215 RCV002560284
dbSNP Id: rs1659097707
COSMIC: COSM43344
MyVariant Identifiers: chr1:g.115256508C>G (hg19) chr1:g.114713887C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713887C>G , CM000663.2:g.114713887C>G GRCh38
NC_000001.10:g.115256508C>G , CM000663.1:g.115256508C>G GRCh37
NC_000001.9:g.115058031C>G NCBI36
NG_007572.1:g.8008G>C , LRG_92:g.8008G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.203G>C MANE Select ENSP00000358548.4:p.Arg68Thr
ENST00000369535.4:c.203G>C ENSP00000358548.4:p.Arg68Thr
NM_002524.4:c.203G>C NP_002515.1:p.Arg68Thr
NM_002524.5:c.203G>C MANE Select NP_002515.1:p.Arg68Thr
Search 100 bp 5'
Search 100 bp 3'