Canonical Allele Identifier: CA2647250826
Gene: NRAS HGNC NCBI

Linked Data

gnomAD v4: 1-114707212-A-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707212A>C , CM000663.2:g.114707212A>C GRCh38
NC_000001.10:g.115249833A>C , CM000663.1:g.115249833A>C GRCh37
NC_000001.9:g.115051356A>C NCBI36
NG_007572.1:g.14683T>G , LRG_92:g.14683T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*882T>G MANE Select ENSP00000358548.4:n.*882T>G
ENST00000369535.4:c.*882T>G ENSP00000358548.4:n.*882T>G
NM_002524.4:c.*882T>G NP_002515.1:n.*882T>G
NM_002524.5:c.*882T>G MANE Select NP_002515.1:n.*882T>G
Search 100 bp 5'
Search 100 bp 3'