Canonical Allele Identifier: CA29039703
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 874294
ClinVar RCV Id: RCV001097130
dbSNP Id: rs370262800
gnomAD v2: 1-115247899-A-G
gnomAD v3: 1-114705278-A-G
gnomAD v4: 1-114705278-A-G
MyVariant Identifiers: chr1:g.115247899A>G (hg19) chr1:g.114705278A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705278A>G , CM000663.2:g.114705278A>G GRCh38
NC_000001.10:g.115247899A>G , CM000663.1:g.115247899A>G GRCh37
NC_000001.9:g.115049422A>G NCBI36
NG_007572.1:g.16617T>C , LRG_92:g.16617T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*2816T>C MANE Select ENSP00000358548.4:n.*2816T>C
ENST00000369535.4:c.*2816T>C ENSP00000358548.4:n.*2816T>C
NM_002524.4:c.*2816T>C NP_002515.1:n.*2816T>C
NM_002524.5:c.*2816T>C MANE Select NP_002515.1:n.*2816T>C
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