Canonical Allele Identifier: CA341741812
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101742168

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713968C>A , CM000663.2:g.114713968C>A GRCh38
NC_000001.10:g.115256589C>A , CM000663.1:g.115256589C>A GRCh37
NC_000001.9:g.115058112C>A NCBI36
NG_007572.1:g.7927G>T , LRG_92:g.7927G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.122G>T MANE Select ENSP00000358548.4:p.Arg41Ile
ENST00000369535.4:c.122G>T ENSP00000358548.4:p.Arg41Ile
NM_002524.4:c.122G>T NP_002515.1:p.Arg41Ile
NM_002524.5:c.122G>T MANE Select NP_002515.1:p.Arg41Ile