Canonical Allele Identifier: CA885830095
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1285654278
MyVariant Identifiers: chr1:g.115256067G>T (hg19) chr1:g.114713446G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713446G>T , CM000663.2:g.114713446G>T GRCh38
NC_000001.10:g.115256067G>T , CM000663.1:g.115256067G>T GRCh37
NC_000001.9:g.115057590G>T NCBI36
NG_007572.1:g.8449C>A , LRG_92:g.8449C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.290+354C>A MANE Select ENSP00000358548.4:n.290+354C>A
ENST00000369535.4:c.290+354C>A ENSP00000358548.4:n.290+354C>A
NM_002524.4:c.290+354C>A NP_002515.1:n.290+354C>A
NM_002524.5:c.290+354C>A MANE Select NP_002515.1:n.290+354C>A
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