Canonical Allele Identifier: CA1190285645
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1658934252
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707037T>G , CM000663.2:g.114707037T>G GRCh38
NC_000001.10:g.115249658T>G , CM000663.1:g.115249658T>G GRCh37
NC_000001.9:g.115051181T>G NCBI36
NG_007572.1:g.14858A>C , LRG_92:g.14858A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*1057A>C MANE Select ENSP00000358548.4:n.*1057A>C
ENST00000369535.4:c.*1057A>C ENSP00000358548.4:n.*1057A>C
NM_002524.4:c.*1057A>C NP_002515.1:n.*1057A>C
NM_002524.5:c.*1057A>C MANE Select NP_002515.1:n.*1057A>C
Search 100 bp 5'
Search 100 bp 3'