Canonical Allele Identifier: CA341741272
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1659096015

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713806A>T , CM000663.2:g.114713806A>T GRCh38
NC_000001.10:g.115256427A>T , CM000663.1:g.115256427A>T GRCh37
NC_000001.9:g.115057950A>T NCBI36
NG_007572.1:g.8089T>A , LRG_92:g.8089T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.284T>A MANE Select ENSP00000358548.4:p.Leu95His
ENST00000369535.4:c.284T>A ENSP00000358548.4:p.Leu95His
NM_002524.4:c.284T>A NP_002515.1:p.Leu95His
NM_002524.5:c.284T>A MANE Select NP_002515.1:p.Leu95His