Canonical Allele Identifier: CA341741302
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101741760
MyVariant Identifiers: chr1:g.115256433A>G (hg19) chr1:g.114713812A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713812A>G , CM000663.2:g.114713812A>G GRCh38
NC_000001.10:g.115256433A>G , CM000663.1:g.115256433A>G GRCh37
NC_000001.9:g.115057956A>G NCBI36
NG_007572.1:g.8083T>C , LRG_92:g.8083T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.278T>C MANE Select ENSP00000358548.4:p.Ile93Thr
ENST00000369535.4:c.278T>C ENSP00000358548.4:p.Ile93Thr
NM_002524.4:c.278T>C NP_002515.1:p.Ile93Thr
NM_002524.5:c.278T>C MANE Select NP_002515.1:p.Ile93Thr
Search 100 bp 5'
Search 100 bp 3'