Canonical Allele Identifier: CA341741639
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 812886
ClinVar RCV Id: RCV001003789 RCV001261065
dbSNP Id: rs1570874751
gnomAD v4: 1-114713914-G-T
COSMIC: COSM253327
MyVariant Identifiers: chr1:g.115256535G>T (hg19) chr1:g.114713914G>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.176C>A MANE Select ENSP00000358548.4:p.Ala59Asp
ENST00000369535.4:c.176C>A ENSP00000358548.4:p.Ala59Asp
NM_002524.4:c.176C>A NP_002515.1:p.Ala59Asp
NM_002524.5:c.176C>A MANE Select NP_002515.1:p.Ala59Asp
Search 100 bp 5'
Search 100 bp 3'