Canonical Allele Identifier: CA29040017
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 876187
ClinVar RCV Id: RCV001100699
dbSNP Id: rs757692247
gnomAD v2: 1-115248303-C-T
gnomAD v3: 1-114705682-C-T
gnomAD v4: 1-114705682-C-T
MyVariant Identifiers: chr1:g.115248303C>T (hg19) chr1:g.114705682C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705682C>T , CM000663.2:g.114705682C>T GRCh38
NC_000001.10:g.115248303C>T , CM000663.1:g.115248303C>T GRCh37
NC_000001.9:g.115049826C>T NCBI36
NG_007572.1:g.16213G>A , LRG_92:g.16213G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2412G>A MANE Select ENSP00000358548.4:n.*2412G>A
ENST00000369535.4:c.*2412G>A ENSP00000358548.4:n.*2412G>A
NM_002524.4:c.*2412G>A NP_002515.1:n.*2412G>A
NM_002524.5:c.*2412G>A MANE Select NP_002515.1:n.*2412G>A
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