Canonical Allele Identifier: CA1190284666
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1570867789

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705689T>G , CM000663.2:g.114705689T>G GRCh38
NC_000001.10:g.115248310T>G , CM000663.1:g.115248310T>G GRCh37
NC_000001.9:g.115049833T>G NCBI36
NG_007572.1:g.16206A>C , LRG_92:g.16206A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2405A>C MANE Select ENSP00000358548.4:n.*2405A>C
ENST00000369535.4:c.*2405A>C ENSP00000358548.4:n.*2405A>C
NM_002524.4:c.*2405A>C NP_002515.1:n.*2405A>C
NM_002524.5:c.*2405A>C MANE Select NP_002515.1:n.*2405A>C