Canonical Allele Identifier: CA341738672

Gene: NRAS

Linked Data

• dbSNP Id: rs367918552
• gnomAD v2: 1-115251222-C-T
• gnomAD v4: 1-114708601-C-T
• MyVariant Identifiers: chr1:g.115251222C>T (hg19) ; chr1:g.114708601C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114708601C>T , CM000663.2:g.114708601C>T	GRCh38
NC_000001.10:g.115251222C>T , CM000663.1:g.115251222C>T	GRCh37
NC_000001.9:g.115052745C>T	NCBI36
NG_007572.1:g.13294G>A , LRG_92:g.13294G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.504G>A MANE Select	ENSP00000358548.4:p.Met168Ile
ENST00000369535.4:c.504G>A	ENSP00000358548.4:p.Met168Ile
NM_002524.4:c.504G>A	NP_002515.1:p.Met168Ile
NM_002524.5:c.504G>A MANE Select	NP_002515.1:p.Met168Ile