Canonical Allele Identifier: CA1190284362
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1658885472
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705348A>C , CM000663.2:g.114705348A>C GRCh38
NC_000001.10:g.115247969A>C , CM000663.1:g.115247969A>C GRCh37
NC_000001.9:g.115049492A>C NCBI36
NG_007572.1:g.16547T>G , LRG_92:g.16547T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*2746T>G MANE Select ENSP00000358548.4:n.*2746T>G
ENST00000369535.4:c.*2746T>G ENSP00000358548.4:n.*2746T>G
NM_002524.4:c.*2746T>G NP_002515.1:n.*2746T>G
NM_002524.5:c.*2746T>G MANE Select NP_002515.1:n.*2746T>G
Search 100 bp 5'
Search 100 bp 3'