Canonical Allele Identifier: CA356968
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 222971
ClinVar RCV Id: RCV000208553 RCV000522652
dbSNP Id: rs869025573
MyVariant Identifiers: chr1:g.115258711A>T (hg19) chr1:g.114716090A>T (hg38)
ERepo: CA356968/MONDO:0021060/039
PubMed: PMID:20301303
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114716090A>T , CM000663.2:g.114716090A>T GRCh38
NC_000001.10:g.115258711A>T , CM000663.1:g.115258711A>T GRCh37
NC_000001.9:g.115060234A>T NCBI36
NG_007572.1:g.5805T>A , LRG_92:g.5805T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.71T>A MANE Select ENSP00000358548.4:p.Ile24Asn
ENST00000369535.4:c.71T>A ENSP00000358548.4:p.Ile24Asn
NM_002524.4:c.71T>A NP_002515.1:p.Ile24Asn
NM_002524.5:c.71T>A MANE Select NP_002515.1:p.Ile24Asn
Search 100 bp 5'
Search 100 bp 3'