Canonical Allele Identifier: CA1020717
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 291976
ClinVar RCV Id: RCV002356400 RCV000262996
dbSNP Id: rs779899354
ExAC: 1:115252260 G / C
gnomAD v2: 1-115252260-G-C
gnomAD v4: 1-114709639-G-C
MyVariant Identifiers: chr1:g.115252260G>C (hg19) chr1:g.114709639G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709639G>C , CM000663.2:g.114709639G>C GRCh38
NC_000001.10:g.115252260G>C , CM000663.1:g.115252260G>C GRCh37
NC_000001.9:g.115053783G>C NCBI36
NG_007572.1:g.12256C>G , LRG_92:g.12256C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.380C>G MANE Select ENSP00000358548.4:p.Thr127Arg
ENST00000369535.4:c.380C>G ENSP00000358548.4:p.Thr127Arg
NM_002524.4:c.380C>G NP_002515.1:p.Thr127Arg
NM_002524.5:c.380C>G MANE Select NP_002515.1:p.Thr127Arg
Search 100 bp 5'
Search 100 bp 3'