Canonical Allele Identifier: CA885826917
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1311786689
gnomAD v4: 1-114707401-T-A
MyVariant Identifiers: chr1:g.115250022T>A (hg19) chr1:g.114707401T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707401T>A , CM000663.2:g.114707401T>A GRCh38
NC_000001.10:g.115250022T>A , CM000663.1:g.115250022T>A GRCh37
NC_000001.9:g.115051545T>A NCBI36
NG_007572.1:g.14494A>T , LRG_92:g.14494A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*693A>T MANE Select ENSP00000358548.4:n.*693A>T
ENST00000369535.4:c.*693A>T ENSP00000358548.4:n.*693A>T
NM_002524.4:c.*693A>T NP_002515.1:n.*693A>T
NM_002524.5:c.*693A>T MANE Select NP_002515.1:n.*693A>T
Search 100 bp 5'
Search 100 bp 3'