Canonical Allele Identifier: CA2647251636
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101737563

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114708096A>C , CM000663.2:g.114708096A>C GRCh38
NC_000001.10:g.115250717A>C , CM000663.1:g.115250717A>C GRCh37
NC_000001.9:g.115052240A>C NCBI36
NG_007572.1:g.13799T>G , LRG_92:g.13799T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*44-46T>G MANE Select ENSP00000358548.4:n.*44-46T>G
ENST00000369535.4:c.*44-46T>G ENSP00000358548.4:n.*44-46T>G
NM_002524.4:c.*44-46T>G NP_002515.1:n.*44-46T>G
NM_002524.5:c.*44-46T>G MANE Select NP_002515.1:n.*44-46T>G