Canonical Allele Identifier: CA1020745
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs764718441

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713810T>G , CM000663.2:g.114713810T>G GRCh38
NC_000001.10:g.115256431T>G , CM000663.1:g.115256431T>G GRCh37
NC_000001.9:g.115057954T>G NCBI36
NG_007572.1:g.8085A>C , LRG_92:g.8085A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.280A>C MANE Select ENSP00000358548.4:p.Asn94His
ENST00000369535.4:c.280A>C ENSP00000358548.4:p.Asn94His
NM_002524.4:c.280A>C NP_002515.1:p.Asn94His
NM_002524.5:c.280A>C MANE Select NP_002515.1:p.Asn94His