Canonical Allele Identifier: CA10607372
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 291961
ClinVar RCV Id: RCV000338787
dbSNP Id: rs886045103
MyVariant Identifiers: chr1:g.115248537C>T (hg19) chr1:g.114705916C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705916C>T , CM000663.2:g.114705916C>T GRCh38
NC_000001.10:g.115248537C>T , CM000663.1:g.115248537C>T GRCh37
NC_000001.9:g.115050060C>T NCBI36
NG_007572.1:g.15979G>A , LRG_92:g.15979G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2178G>A MANE Select ENSP00000358548.4:n.*2178G>A
ENST00000369535.4:c.*2178G>A ENSP00000358548.4:n.*2178G>A
NM_002524.4:c.*2178G>A NP_002515.1:n.*2178G>A
NM_002524.5:c.*2178G>A MANE Select NP_002515.1:n.*2178G>A
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