Canonical Allele Identifier: CA341741403
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2054868
ClinVar RCV Id: RCV003317628 RCV002933042
dbSNP Id: rs1659096732
gnomAD v3: 1-114713831-T-A
gnomAD v4: 1-114713831-T-A
COSMIC: COSM5044301
MyVariant Identifiers: chr1:g.115256452T>A (hg19) chr1:g.114713831T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713831T>A , CM000663.2:g.114713831T>A GRCh38
NC_000001.10:g.115256452T>A , CM000663.1:g.115256452T>A GRCh37
NC_000001.9:g.115057975T>A NCBI36
NG_007572.1:g.8064A>T , LRG_92:g.8064A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.259A>T MANE Select ENSP00000358548.4:p.Ser87Cys
ENST00000369535.4:c.259A>T ENSP00000358548.4:p.Ser87Cys
NM_002524.4:c.259A>T NP_002515.1:p.Ser87Cys
NM_002524.5:c.259A>T MANE Select NP_002515.1:p.Ser87Cys
Search 100 bp 5'
Search 100 bp 3'