Canonical Allele Identifier: CA341741638
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1570874751
COSMIC: COSM5878737
MyVariant Identifiers: chr1:g.115256535G>C (hg19) chr1:g.114713914G>C (hg38)
PubMed: PMID:28135719
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713914G>C , CM000663.2:g.114713914G>C GRCh38
NC_000001.10:g.115256535G>C , CM000663.1:g.115256535G>C GRCh37
NC_000001.9:g.115058058G>C NCBI36
NG_007572.1:g.7981C>G , LRG_92:g.7981C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.176C>G MANE Select ENSP00000358548.4:p.Ala59Gly
ENST00000369535.4:c.176C>G ENSP00000358548.4:p.Ala59Gly
NM_002524.4:c.176C>G NP_002515.1:p.Ala59Gly
NM_002524.5:c.176C>G MANE Select NP_002515.1:p.Ala59Gly
Search 100 bp 5'
Search 100 bp 3'