Canonical Allele Identifier: CA341741443
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1365997556
gnomAD v2: 1-115256459-G-C
gnomAD v4: 1-114713838-G-C
MyVariant Identifiers: chr1:g.115256459G>C (hg19) chr1:g.114713838G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713838G>C , CM000663.2:g.114713838G>C GRCh38
NC_000001.10:g.115256459G>C , CM000663.1:g.115256459G>C GRCh37
NC_000001.9:g.115057982G>C NCBI36
NG_007572.1:g.8057C>G , LRG_92:g.8057C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.252C>G MANE Select ENSP00000358548.4:p.Ile84Met
ENST00000369535.4:c.252C>G ENSP00000358548.4:p.Ile84Met
NM_002524.4:c.252C>G NP_002515.1:p.Ile84Met
NM_002524.5:c.252C>G MANE Select NP_002515.1:p.Ile84Met
Search 100 bp 5'
Search 100 bp 3'