Canonical Allele Identifier: CA1005997560
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1658942041
gnomAD v3: 1-114707400-A-T
gnomAD v4: 1-114707400-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707400A>T , CM000663.2:g.114707400A>T GRCh38
NC_000001.10:g.115250021A>T , CM000663.1:g.115250021A>T GRCh37
NC_000001.9:g.115051544A>T NCBI36
NG_007572.1:g.14495T>A , LRG_92:g.14495T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*694T>A MANE Select ENSP00000358548.4:n.*694T>A
ENST00000369535.4:c.*694T>A ENSP00000358548.4:n.*694T>A
NM_002524.4:c.*694T>A NP_002515.1:n.*694T>A
NM_002524.5:c.*694T>A MANE Select NP_002515.1:n.*694T>A
Search 100 bp 5'
Search 100 bp 3'