Canonical Allele Identifier: CA525631037
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1485843761

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114714012A>G , CM000663.2:g.114714012A>G GRCh38
NC_000001.10:g.115256633A>G , CM000663.1:g.115256633A>G GRCh37
NC_000001.9:g.115058156A>G NCBI36
NG_007572.1:g.7883T>C , LRG_92:g.7883T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-34T>C MANE Select ENSP00000358548.4:n.112-34T>C
ENST00000369535.4:c.112-34T>C ENSP00000358548.4:n.112-34T>C
NM_002524.4:c.112-34T>C NP_002515.1:n.112-34T>C
NM_002524.5:c.112-34T>C MANE Select NP_002515.1:n.112-34T>C