Canonical Allele Identifier: CA419887167
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1723142
ClinVar RCV Id: RCV002306249
MyVariant Identifiers: chr1:g.115256531T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713910T>C , CM000663.2:g.114713910T>C GRCh38
NC_000001.10:g.115256531T>C , CM000663.1:g.115256531T>C GRCh37
NC_000001.9:g.115058054T>C NCBI36
NG_007572.1:g.7985A>G , LRG_92:g.7985A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.180A>G MANE Select ENSP00000358548.4:p.Gly60=
ENST00000369535.4:c.180A>G ENSP00000358548.4:p.Gly60=
NM_002524.4:c.180A>G NP_002515.1:p.Gly60=
NM_002524.5:c.180A>G MANE Select NP_002515.1:p.Gly60=