Canonical Allele Identifier: CA2647250675
Gene: NRAS HGNC NCBI

Linked Data

gnomAD v4: 1-114706898-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114706898G>T , CM000663.2:g.114706898G>T GRCh38
NC_000001.10:g.115249519G>T , CM000663.1:g.115249519G>T GRCh37
NC_000001.9:g.115051042G>T NCBI36
NG_007572.1:g.14997C>A , LRG_92:g.14997C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*1196C>A MANE Select ENSP00000358548.4:n.*1196C>A
ENST00000369535.4:c.*1196C>A ENSP00000358548.4:n.*1196C>A
NM_002524.4:c.*1196C>A NP_002515.1:n.*1196C>A
NM_002524.5:c.*1196C>A MANE Select NP_002515.1:n.*1196C>A
Search 100 bp 5'
Search 100 bp 3'