Canonical Allele Identifier: CA16602496
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 376027
ClinVar RCV Id: RCV000425052
dbSNP Id: rs121913254
gnomAD v4: 1-114713909-G-A
COSMIC: COSM6005482
MyVariant Identifiers: chr1:g.115256530G>A (hg19) chr1:g.114713909G>A (hg38)
PubMed: PMID:23076151 PMID:25157968
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713909G>A , CM000663.2:g.114713909G>A GRCh38
NC_000001.10:g.115256530G>A , CM000663.1:g.115256530G>A GRCh37
NC_000001.9:g.115058053G>A NCBI36
NG_007572.1:g.7986C>T , LRG_92:g.7986C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.181C>T MANE Select ENSP00000358548.4:p.Gln61Ter
ENST00000369535.4:c.181C>T ENSP00000358548.4:p.Gln61Ter
NM_002524.4:c.181C>T NP_002515.1:p.Gln61Ter
NM_002524.5:c.181C>T MANE Select NP_002515.1:p.Gln61Ter
Search 100 bp 5'
Search 100 bp 3'