Canonical Allele Identifier: CA2696724001
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101737023
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707152T>G , CM000663.2:g.114707152T>G GRCh38
NC_000001.10:g.115249773T>G , CM000663.1:g.115249773T>G GRCh37
NC_000001.9:g.115051296T>G NCBI36
NG_007572.1:g.14743A>C , LRG_92:g.14743A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*942A>C MANE Select ENSP00000358548.4:n.*942A>C
ENST00000369535.4:c.*942A>C ENSP00000358548.4:n.*942A>C
NM_002524.4:c.*942A>C NP_002515.1:n.*942A>C
NM_002524.5:c.*942A>C MANE Select NP_002515.1:n.*942A>C
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