Canonical Allele Identifier: CA1190284367
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1658885658
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705356C>A , CM000663.2:g.114705356C>A GRCh38
NC_000001.10:g.115247977C>A , CM000663.1:g.115247977C>A GRCh37
NC_000001.9:g.115049500C>A NCBI36
NG_007572.1:g.16539G>T , LRG_92:g.16539G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*2738G>T MANE Select ENSP00000358548.4:n.*2738G>T
ENST00000369535.4:c.*2738G>T ENSP00000358548.4:n.*2738G>T
NM_002524.4:c.*2738G>T NP_002515.1:n.*2738G>T
NM_002524.5:c.*2738G>T MANE Select NP_002515.1:n.*2738G>T
Search 100 bp 5'
Search 100 bp 3'