Canonical Allele Identifier: CA885830166
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1210222919
gnomAD v3: 1-114713725-T-G
gnomAD v4: 1-114713725-T-G
MyVariant Identifiers: chr1:g.115256346T>G (hg19) chr1:g.114713725T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713725T>G , CM000663.2:g.114713725T>G GRCh38
NC_000001.10:g.115256346T>G , CM000663.1:g.115256346T>G GRCh37
NC_000001.9:g.115057869T>G NCBI36
NG_007572.1:g.8170A>C , LRG_92:g.8170A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.290+75A>C MANE Select ENSP00000358548.4:n.290+75A>C
ENST00000369535.4:c.290+75A>C ENSP00000358548.4:n.290+75A>C
NM_002524.4:c.290+75A>C NP_002515.1:n.290+75A>C
NM_002524.5:c.290+75A>C MANE Select NP_002515.1:n.290+75A>C
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