Canonical Allele Identifier: CA341739589

Gene: NRAS

Linked Data

• dbSNP Id: rs1198714974
• gnomAD v2: 1-115252307-C-A
• gnomAD v4: 1-114709686-C-A
• MyVariant Identifiers: chr1:g.115252307C>A (hg19) ; chr1:g.114709686C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709686C>A , CM000663.2:g.114709686C>A	GRCh38
NC_000001.10:g.115252307C>A , CM000663.1:g.115252307C>A	GRCh37
NC_000001.9:g.115053830C>A	NCBI36
NG_007572.1:g.12209G>T , LRG_92:g.12209G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.333G>T MANE Select	ENSP00000358548.4:p.Met111Ile
ENST00000369535.4:c.333G>T	ENSP00000358548.4:p.Met111Ile
NM_002524.4:c.333G>T	NP_002515.1:p.Met111Ile
NM_002524.5:c.333G>T MANE Select	NP_002515.1:p.Met111Ile