Canonical Allele Identifier: CA1020690
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 450081
ClinVar RCV Id: RCV000521930 RCV002527601
dbSNP Id: rs747080102
ExAC: 1:115251262 G / A
gnomAD v2: 1-115251262-G-A
gnomAD v3: 1-114708641-G-A
gnomAD v4: 1-114708641-G-A
MyVariant Identifiers: chr1:g.115251262G>A (hg19) chr1:g.114708641G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114708641G>A , CM000663.2:g.114708641G>A GRCh38
NC_000001.10:g.115251262G>A , CM000663.1:g.115251262G>A GRCh37
NC_000001.9:g.115052785G>A NCBI36
NG_007572.1:g.13254C>T , LRG_92:g.13254C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.464C>T MANE Select ENSP00000358548.4:p.Ala155Val
ENST00000369535.4:c.464C>T ENSP00000358548.4:p.Ala155Val
NM_002524.4:c.464C>T NP_002515.1:p.Ala155Val
NM_002524.5:c.464C>T MANE Select NP_002515.1:p.Ala155Val
Search 100 bp 5'
Search 100 bp 3'