Canonical Allele Identifier: CA1020708
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2739681
ClinVar RCV Id: RCV003540189
dbSNP Id: rs765687422
ExAC: 1:115252187 T / C
gnomAD v2: 1-115252187-T-C
gnomAD v4: 1-114709566-T-C
MyVariant Identifiers: chr1:g.115252187T>C (hg19) chr1:g.114709566T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709566T>C , CM000663.2:g.114709566T>C GRCh38
NC_000001.10:g.115252187T>C , CM000663.1:g.115252187T>C GRCh37
NC_000001.9:g.115053710T>C NCBI36
NG_007572.1:g.12329A>G , LRG_92:g.12329A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.450+3A>G MANE Select ENSP00000358548.4:n.450+3A>G
ENST00000369535.4:c.450+3A>G ENSP00000358548.4:n.450+3A>G
NM_002524.4:c.450+3A>G NP_002515.1:n.450+3A>G
NM_002524.5:c.450+3A>G MANE Select NP_002515.1:n.450+3A>G
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