Canonical Allele Identifier: CA161312
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 134991
ClinVar RCV Id: RCV000121741 RCV000680367
dbSNP Id: rs367918552
ExAC: 1:115251222 C / G
gnomAD v2: 1-115251222-C-G
gnomAD v3: 1-114708601-C-G
gnomAD v4: 1-114708601-C-G
MyVariant Identifiers: chr1:g.115251222C>G (hg19) chr1:g.114708601C>G (hg38)
PubMed: PMID:24728327
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114708601C>G , CM000663.2:g.114708601C>G GRCh38
NC_000001.10:g.115251222C>G , CM000663.1:g.115251222C>G GRCh37
NC_000001.9:g.115052745C>G NCBI36
NG_007572.1:g.13294G>C , LRG_92:g.13294G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.504G>C MANE Select ENSP00000358548.4:p.Met168Ile
ENST00000369535.4:c.504G>C ENSP00000358548.4:p.Met168Ile
NM_002524.4:c.504G>C NP_002515.1:p.Met168Ile
NM_002524.5:c.504G>C MANE Select NP_002515.1:p.Met168Ile
Search 100 bp 5'
Search 100 bp 3'