Canonical Allele Identifier: CA341741263
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101741734
COSMIC: COSM5546656
MyVariant Identifiers: chr1:g.115256422T>C (hg19) chr1:g.114713801T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713801T>C , CM000663.2:g.114713801T>C GRCh38
NC_000001.10:g.115256422T>C , CM000663.1:g.115256422T>C GRCh37
NC_000001.9:g.115057945T>C NCBI36
NG_007572.1:g.8094A>G , LRG_92:g.8094A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.289A>G MANE Select ENSP00000358548.4:p.Arg97Gly
ENST00000369535.4:c.289A>G ENSP00000358548.4:p.Arg97Gly
NM_002524.4:c.289A>G NP_002515.1:p.Arg97Gly
NM_002524.5:c.289A>G MANE Select NP_002515.1:p.Arg97Gly
Search 100 bp 5'
Search 100 bp 3'