Canonical Allele Identifier: CA341742733
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 477662
ClinVar RCV Id: RCV000545519 RCV002476203
dbSNP Id: rs1553244682
gnomAD v4: 1-114716136-C-T
COSMIC: COSM6438071
MyVariant Identifiers: chr1:g.115258757C>T (hg19) chr1:g.114716136C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114716136C>T , CM000663.2:g.114716136C>T GRCh38
NC_000001.10:g.115258757C>T , CM000663.1:g.115258757C>T GRCh37
NC_000001.9:g.115060280C>T NCBI36
NG_007572.1:g.5759G>A , LRG_92:g.5759G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.25G>A MANE Select ENSP00000358548.4:p.Val9Ile
ENST00000369535.4:c.25G>A ENSP00000358548.4:p.Val9Ile
NM_002524.4:c.25G>A NP_002515.1:p.Val9Ile
NM_002524.5:c.25G>A MANE Select NP_002515.1:p.Val9Ile
Search 100 bp 5'
Search 100 bp 3'