Canonical Allele Identifier: CA341741346
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101741786
MyVariant Identifiers: chr1:g.115256441A>T (hg19) chr1:g.114713820A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713820A>T , CM000663.2:g.114713820A>T GRCh38
NC_000001.10:g.115256441A>T , CM000663.1:g.115256441A>T GRCh37
NC_000001.9:g.115057964A>T NCBI36
NG_007572.1:g.8075T>A , LRG_92:g.8075T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.270T>A MANE Select ENSP00000358548.4:p.Phe90Leu
ENST00000369535.4:c.270T>A ENSP00000358548.4:p.Phe90Leu
NM_002524.4:c.270T>A NP_002515.1:p.Phe90Leu
NM_002524.5:c.270T>A MANE Select NP_002515.1:p.Phe90Leu
Search 100 bp 5'
Search 100 bp 3'