Canonical Allele Identifier: CA1005997511
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1658937361

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707204T>C , CM000663.2:g.114707204T>C GRCh38
NC_000001.10:g.115249825T>C , CM000663.1:g.115249825T>C GRCh37
NC_000001.9:g.115051348T>C NCBI36
NG_007572.1:g.14691A>G , LRG_92:g.14691A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*890A>G MANE Select ENSP00000358548.4:n.*890A>G
ENST00000369535.4:c.*890A>G ENSP00000358548.4:n.*890A>G
NM_002524.4:c.*890A>G NP_002515.1:n.*890A>G
NM_002524.5:c.*890A>G MANE Select NP_002515.1:n.*890A>G