Canonical Allele Identifier: CA2696725970
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101741613
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713748A>T , CM000663.2:g.114713748A>T GRCh38
NC_000001.10:g.115256369A>T , CM000663.1:g.115256369A>T GRCh37
NC_000001.9:g.115057892A>T NCBI36
NG_007572.1:g.8147T>A , LRG_92:g.8147T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.290+52T>A MANE Select ENSP00000358548.4:n.290+52T>A
ENST00000369535.4:c.290+52T>A ENSP00000358548.4:n.290+52T>A
NM_002524.4:c.290+52T>A NP_002515.1:n.290+52T>A
NM_002524.5:c.290+52T>A MANE Select NP_002515.1:n.290+52T>A
Search 100 bp 5'
Search 100 bp 3'