Canonical Allele Identifier: CA1020759

Gene: NRAS

Linked Data

• ClinVar Variation Id: 876240
• ClinVar RCV Id: RCV001100798 ; RCV001566706 ; RCV002558012
• dbSNP Id: rs200604652
• ExAC: 1:115256605 G / C
• gnomAD v2: 1-115256605-G-C
• gnomAD v3: 1-114713984-G-C
• gnomAD v4: 1-114713984-G-C
• MyVariant Identifiers: chr1:g.115256605G>C (hg19) ; chr1:g.114713984G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713984G>C , CM000663.2:g.114713984G>C	GRCh38
NC_000001.10:g.115256605G>C , CM000663.1:g.115256605G>C	GRCh37
NC_000001.9:g.115058128G>C	NCBI36
NG_007572.1:g.7911C>G , LRG_92:g.7911C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.112-6C>G MANE Select	ENSP00000358548.4:n.112-6C>G
ENST00000369535.4:c.112-6C>G	ENSP00000358548.4:n.112-6C>G
NM_002524.4:c.112-6C>G	NP_002515.1:n.112-6C>G
NM_002524.5:c.112-6C>G MANE Select	NP_002515.1:n.112-6C>G