Canonical Allele Identifier: CA885828570
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs7549358
MyVariant Identifiers: chr1:g.115252609G>T (hg19) chr1:g.114709988G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709988G>T , CM000663.2:g.114709988G>T GRCh38
NC_000001.10:g.115252609G>T , CM000663.1:g.115252609G>T GRCh37
NC_000001.9:g.115054132G>T NCBI36
NG_007572.1:g.11907C>A , LRG_92:g.11907C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.291-260C>A MANE Select ENSP00000358548.4:n.291-260C>A
ENST00000369535.4:c.291-260C>A ENSP00000358548.4:n.291-260C>A
NM_002524.4:c.291-260C>A NP_002515.1:n.291-260C>A
NM_002524.5:c.291-260C>A MANE Select NP_002515.1:n.291-260C>A
Search 100 bp 5'
Search 100 bp 3'