Canonical Allele Identifier: CA341741631
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101742004
gnomAD v4: 1-114713906-C-T
COSMIC: COSM6438070
MyVariant Identifiers: chr1:g.115256527C>T (hg19) chr1:g.114713906C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713906C>T , CM000663.2:g.114713906C>T GRCh38
NC_000001.10:g.115256527C>T , CM000663.1:g.115256527C>T GRCh37
NC_000001.9:g.115058050C>T NCBI36
NG_007572.1:g.7989G>A , LRG_92:g.7989G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.184G>A MANE Select ENSP00000358548.4:p.Glu62Lys
ENST00000369535.4:c.184G>A ENSP00000358548.4:p.Glu62Lys
NM_002524.4:c.184G>A NP_002515.1:p.Glu62Lys
NM_002524.5:c.184G>A MANE Select NP_002515.1:p.Glu62Lys
Search 100 bp 5'
Search 100 bp 3'