Canonical Allele Identifier: CA2696725460
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101738497
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709527C>G , CM000663.2:g.114709527C>G GRCh38
NC_000001.10:g.115252148C>G , CM000663.1:g.115252148C>G GRCh37
NC_000001.9:g.115053671C>G NCBI36
NG_007572.1:g.12368G>C , LRG_92:g.12368G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.450+42G>C MANE Select ENSP00000358548.4:n.450+42G>C
ENST00000369535.4:c.450+42G>C ENSP00000358548.4:n.450+42G>C
NM_002524.4:c.450+42G>C NP_002515.1:n.450+42G>C
NM_002524.5:c.450+42G>C MANE Select NP_002515.1:n.450+42G>C
Search 100 bp 5'
Search 100 bp 3'