Canonical Allele Identifier: CA292582

Gene: NRAS

Linked Data

• ClinVar Variation Id: 138538
• ClinVar RCV Id: RCV000127228 ; RCV000588495 ; RCV001101050 ; RCV001089307 ; RCV001813388 ; RCV003905211
• dbSNP Id: rs9724626
• ExAC: 1:115256607 T / C
• gnomAD v2: 1-115256607-T-C
• gnomAD v3: 1-114713986-T-C
• gnomAD v4: 1-114713986-T-C
• MyVariant Identifiers: chr1:g.115256607T>C (hg19) ; chr1:g.114713986T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713986T>C , CM000663.2:g.114713986T>C	GRCh38
NC_000001.10:g.115256607T>C , CM000663.1:g.115256607T>C	GRCh37
NC_000001.9:g.115058130T>C	NCBI36
NG_007572.1:g.7909A>G , LRG_92:g.7909A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.112-8A>G MANE Select	ENSP00000358548.4:n.112-8A>G
ENST00000369535.4:c.112-8A>G	ENSP00000358548.4:n.112-8A>G
NM_002524.4:c.112-8A>G	NP_002515.1:n.112-8A>G
NM_002524.5:c.112-8A>G MANE Select	NP_002515.1:n.112-8A>G