Canonical Allele Identifier: CA1005997523
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1658939341
gnomAD v3: 1-114707281-T-G
gnomAD v4: 1-114707281-T-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707281T>G , CM000663.2:g.114707281T>G GRCh38
NC_000001.10:g.115249902T>G , CM000663.1:g.115249902T>G GRCh37
NC_000001.9:g.115051425T>G NCBI36
NG_007572.1:g.14614A>C , LRG_92:g.14614A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*813A>C MANE Select ENSP00000358548.4:n.*813A>C
ENST00000369535.4:c.*813A>C ENSP00000358548.4:n.*813A>C
NM_002524.4:c.*813A>C NP_002515.1:n.*813A>C
NM_002524.5:c.*813A>C MANE Select NP_002515.1:n.*813A>C
Search 100 bp 5'
Search 100 bp 3'