Canonical Allele Identifier: CA341741660
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2746485
ClinVar RCV Id: RCV003540240
dbSNP Id: rs758182152
gnomAD v4: 1-114713924-G-C
MyVariant Identifiers: chr1:g.115256545G>C (hg19) chr1:g.114713924G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713924G>C , CM000663.2:g.114713924G>C GRCh38
NC_000001.10:g.115256545G>C , CM000663.1:g.115256545G>C GRCh37
NC_000001.9:g.115058068G>C NCBI36
NG_007572.1:g.7971C>G , LRG_92:g.7971C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.166C>G MANE Select ENSP00000358548.4:p.Leu56Val
ENST00000369535.4:c.166C>G ENSP00000358548.4:p.Leu56Val
NM_002524.4:c.166C>G NP_002515.1:p.Leu56Val
NM_002524.5:c.166C>G MANE Select NP_002515.1:p.Leu56Val
Search 100 bp 5'
Search 100 bp 3'