Canonical Allele Identifier: CA10607699
Gene: NRAS HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.114707748C>T
GRCh37 chr1:g.115250369C>T
gnomAD v2:
1:115250369 C / T
gnomAD v3:
1:114707748 C / T
gnomAD v4:
chr1-114707748-C-T
Joint Max Group AF 0.05583423 (SAS)
Genomes Max Group AF 0.05583423 (SAS)
ClinVar RCV:
RCV000370376
ClinVar Variation:
291973
dbSNP:
9724642
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707748C>T , CM000663.2:g.114707748C>T GRCh38
NC_000001.10:g.115250369C>T , CM000663.1:g.115250369C>T GRCh37
NC_000001.9:g.115051892C>T NCBI36
NG_007572.1:g.14147G>A , LRG_92:g.14147G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*346G>A MANE Select ENSP00000358548.4:n.*346G>A
ENST00000369535.4:c.*346G>A ENSP00000358548.4:n.*346G>A
NM_002524.4:c.*346G>A NP_002515.1:n.*346G>A
NM_002524.5:c.*346G>A MANE Select NP_002515.1:n.*346G>A
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