Canonical Allele Identifier: CA161312

Gene: NRAS

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

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