Canonical Allele Identifier: CA341739820
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101739009
MyVariant Identifiers: chr1:g.115252348C>T (hg19) chr1:g.114709727C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709727C>T , CM000663.2:g.114709727C>T GRCh38
NC_000001.10:g.115252348C>T , CM000663.1:g.115252348C>T GRCh37
NC_000001.9:g.115053871C>T NCBI36
NG_007572.1:g.12168G>A , LRG_92:g.12168G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.292G>A MANE Select ENSP00000358548.4:p.Glu98Lys
ENST00000369535.4:c.292G>A ENSP00000358548.4:p.Glu98Lys
NM_002524.4:c.292G>A NP_002515.1:p.Glu98Lys
NM_002524.5:c.292G>A MANE Select NP_002515.1:p.Glu98Lys
Search 100 bp 5'
Search 100 bp 3'