Canonical Allele Identifier: CA2696725254
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101738427
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709494A>T , CM000663.2:g.114709494A>T GRCh38
NC_000001.10:g.115252115A>T , CM000663.1:g.115252115A>T GRCh37
NC_000001.9:g.115053638A>T NCBI36
NG_007572.1:g.12401T>A , LRG_92:g.12401T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.450+75T>A MANE Select ENSP00000358548.4:n.450+75T>A
ENST00000369535.4:c.450+75T>A ENSP00000358548.4:n.450+75T>A
NM_002524.4:c.450+75T>A NP_002515.1:n.450+75T>A
NM_002524.5:c.450+75T>A MANE Select NP_002515.1:n.450+75T>A
Search 100 bp 5'
Search 100 bp 3'