Canonical Allele Identifier: CA1190285475
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1658929855
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114706820C>T , CM000663.2:g.114706820C>T GRCh38
NC_000001.10:g.115249441C>T , CM000663.1:g.115249441C>T GRCh37
NC_000001.9:g.115050964C>T NCBI36
NG_007572.1:g.15075G>A , LRG_92:g.15075G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*1274G>A MANE Select ENSP00000358548.4:n.*1274G>A
ENST00000369535.4:c.*1274G>A ENSP00000358548.4:n.*1274G>A
NM_002524.4:c.*1274G>A NP_002515.1:n.*1274G>A
NM_002524.5:c.*1274G>A MANE Select NP_002515.1:n.*1274G>A
Search 100 bp 5'
Search 100 bp 3'