Canonical Allele Identifier: CA29039729
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 874296
ClinVar RCV Id: RCV001097132
dbSNP Id: rs766572336
gnomAD v2: 1-115247948-G-A
gnomAD v3: 1-114705327-G-A
gnomAD v4: 1-114705327-G-A
MyVariant Identifiers: chr1:g.115247948G>A (hg19) chr1:g.114705327G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705327G>A , CM000663.2:g.114705327G>A GRCh38
NC_000001.10:g.115247948G>A , CM000663.1:g.115247948G>A GRCh37
NC_000001.9:g.115049471G>A NCBI36
NG_007572.1:g.16568C>T , LRG_92:g.16568C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*2767C>T MANE Select ENSP00000358548.4:n.*2767C>T
ENST00000369535.4:c.*2767C>T ENSP00000358548.4:n.*2767C>T
NM_002524.4:c.*2767C>T NP_002515.1:n.*2767C>T
NM_002524.5:c.*2767C>T MANE Select NP_002515.1:n.*2767C>T
Search 100 bp 5'
Search 100 bp 3'