Canonical Allele Identifier: CA525408254
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1306896728

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707224G>A , CM000663.2:g.114707224G>A GRCh38
NC_000001.10:g.115249845G>A , CM000663.1:g.115249845G>A GRCh37
NC_000001.9:g.115051368G>A NCBI36
NG_007572.1:g.14671C>T , LRG_92:g.14671C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*870C>T MANE Select ENSP00000358548.4:n.*870C>T
ENST00000369535.4:c.*870C>T ENSP00000358548.4:n.*870C>T
NM_002524.4:c.*870C>T NP_002515.1:n.*870C>T
NM_002524.5:c.*870C>T MANE Select NP_002515.1:n.*870C>T