Canonical Allele Identifier: CA10607488
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 291970
ClinVar RCV Id: RCV000367629
dbSNP Id: rs555171083
gnomAD v2: 1-115250132-A-C
gnomAD v3: 1-114707511-A-C
gnomAD v4: 1-114707511-A-C
MyVariant Identifiers: chr1:g.115250132A>C (hg19) chr1:g.114707511A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707511A>C , CM000663.2:g.114707511A>C GRCh38
NC_000001.10:g.115250132A>C , CM000663.1:g.115250132A>C GRCh37
NC_000001.9:g.115051655A>C NCBI36
NG_007572.1:g.14384T>G , LRG_92:g.14384T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*583T>G MANE Select ENSP00000358548.4:n.*583T>G
ENST00000369535.4:c.*583T>G ENSP00000358548.4:n.*583T>G
NM_002524.4:c.*583T>G NP_002515.1:n.*583T>G
NM_002524.5:c.*583T>G MANE Select NP_002515.1:n.*583T>G
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