Canonical Allele Identifier: CA341741356
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1320040
ClinVar RCV Id: RCV001775214 RCV003154193
dbSNP Id: rs1393160852
gnomAD v2: 1-115256443-A-G
MyVariant Identifiers: chr1:g.115256443A>G (hg19) chr1:g.114713822A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713822A>G , CM000663.2:g.114713822A>G GRCh38
NC_000001.10:g.115256443A>G , CM000663.1:g.115256443A>G GRCh37
NC_000001.9:g.115057966A>G NCBI36
NG_007572.1:g.8073T>C , LRG_92:g.8073T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.268T>C MANE Select ENSP00000358548.4:p.Phe90Leu
ENST00000369535.4:c.268T>C ENSP00000358548.4:p.Phe90Leu
NM_002524.4:c.268T>C NP_002515.1:p.Phe90Leu
NM_002524.5:c.268T>C MANE Select NP_002515.1:p.Phe90Leu
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