Canonical Allele Identifier: CA341741330
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1334643
ClinVar RCV Id: RCV001814824
dbSNP Id: rs2101741771
COSMIC: COSM43346
MyVariant Identifiers: chr1:g.115256437C>T (hg19) chr1:g.114713816C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713816C>T , CM000663.2:g.114713816C>T GRCh38
NC_000001.10:g.115256437C>T , CM000663.1:g.115256437C>T GRCh37
NC_000001.9:g.115057960C>T NCBI36
NG_007572.1:g.8079G>A , LRG_92:g.8079G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.274G>A MANE Select ENSP00000358548.4:p.Asp92Asn
ENST00000369535.4:c.274G>A ENSP00000358548.4:p.Asp92Asn
NM_002524.4:c.274G>A NP_002515.1:p.Asp92Asn
NM_002524.5:c.274G>A MANE Select NP_002515.1:p.Asp92Asn
Search 100 bp 5'
Search 100 bp 3'