Canonical Allele Identifier: CA341741485
Gene: NRAS HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.115256467A>T (hg19) chr1:g.114713846A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713846A>T , CM000663.2:g.114713846A>T GRCh38
NC_000001.10:g.115256467A>T , CM000663.1:g.115256467A>T GRCh37
NC_000001.9:g.115057990A>T NCBI36
NG_007572.1:g.8049T>A , LRG_92:g.8049T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.244T>A MANE Select ENSP00000358548.4:p.Phe82Ile
ENST00000369535.4:c.244T>A ENSP00000358548.4:p.Phe82Ile
NM_002524.4:c.244T>A NP_002515.1:p.Phe82Ile
NM_002524.5:c.244T>A MANE Select NP_002515.1:p.Phe82Ile
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