Canonical Allele Identifier: CA257021
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 13903
ClinVar RCV Id: RCV000014917 RCV000158982 RCV000208552 RCV001382056 RCV003415702
dbSNP Id: rs267606920
gnomAD v2: 1-115256532-C-T
gnomAD v3: 1-114713911-C-T
gnomAD v4: 1-114713911-C-T
COSMIC: COSM28673
MyVariant Identifiers: chr1:g.115256532C>T (hg19) chr1:g.114713911C>T (hg38)
PubMed: PMID:19966803 PMID:20301303 PMID:26467218
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713911C>T , CM000663.2:g.114713911C>T GRCh38
NC_000001.10:g.115256532C>T , CM000663.1:g.115256532C>T GRCh37
NC_000001.9:g.115058055C>T NCBI36
NG_007572.1:g.7984G>A , LRG_92:g.7984G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.179G>A MANE Select ENSP00000358548.4:p.Gly60Glu
ENST00000369535.4:c.179G>A ENSP00000358548.4:p.Gly60Glu
NM_002524.4:c.179G>A NP_002515.1:p.Gly60Glu
NM_002524.5:c.179G>A MANE Select NP_002515.1:p.Gly60Glu
Search 100 bp 5'
Search 100 bp 3'