Canonical Allele Identifier: CA1020740
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs746512237

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713769A>G , CM000663.2:g.114713769A>G GRCh38
NC_000001.10:g.115256390A>G , CM000663.1:g.115256390A>G GRCh37
NC_000001.9:g.115057913A>G NCBI36
NG_007572.1:g.8126T>C , LRG_92:g.8126T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.290+31T>C MANE Select ENSP00000358548.4:n.290+31T>C
ENST00000369535.4:c.290+31T>C ENSP00000358548.4:n.290+31T>C
NM_002524.4:c.290+31T>C NP_002515.1:n.290+31T>C
NM_002524.5:c.290+31T>C MANE Select NP_002515.1:n.290+31T>C