Canonical Allele Identifier: CA1190284335
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs889526788
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705314T>A , CM000663.2:g.114705314T>A GRCh38
NC_000001.10:g.115247935T>A , CM000663.1:g.115247935T>A GRCh37
NC_000001.9:g.115049458T>A NCBI36
NG_007572.1:g.16581A>T , LRG_92:g.16581A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*2780A>T MANE Select ENSP00000358548.4:n.*2780A>T
ENST00000369535.4:c.*2780A>T ENSP00000358548.4:n.*2780A>T
NM_002524.4:c.*2780A>T NP_002515.1:n.*2780A>T
NM_002524.5:c.*2780A>T MANE Select NP_002515.1:n.*2780A>T
Search 100 bp 5'
Search 100 bp 3'