Canonical Allele Identifier: CA341741494
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101741844
MyVariant Identifiers: chr1:g.115256472C>A (hg19) chr1:g.114713851C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713851C>A , CM000663.2:g.114713851C>A GRCh38
NC_000001.10:g.115256472C>A , CM000663.1:g.115256472C>A GRCh37
NC_000001.9:g.115057995C>A NCBI36
NG_007572.1:g.8044G>T , LRG_92:g.8044G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.239G>T MANE Select ENSP00000358548.4:p.Cys80Phe
ENST00000369535.4:c.239G>T ENSP00000358548.4:p.Cys80Phe
NM_002524.4:c.239G>T NP_002515.1:p.Cys80Phe
NM_002524.5:c.239G>T MANE Select NP_002515.1:p.Cys80Phe
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