Canonical Allele Identifier: CA10607646
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 291943
ClinVar RCV Id: RCV000278492
dbSNP Id: rs72994440
gnomAD v2: 1-115247349-C-A
gnomAD v3: 1-114704728-C-A
gnomAD v4: 1-114704728-C-A
MyVariant Identifiers: chr1:g.115247349C>A (hg19) chr1:g.114704728C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114704728C>A , CM000663.2:g.114704728C>A GRCh38
NC_000001.10:g.115247349C>A , CM000663.1:g.115247349C>A GRCh37
NC_000001.9:g.115048872C>A NCBI36
NG_007572.1:g.17167G>T , LRG_92:g.17167G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*3366G>T MANE Select ENSP00000358548.4:n.*3366G>T
ENST00000369535.4:c.*3366G>T ENSP00000358548.4:n.*3366G>T
NM_002524.4:c.*3366G>T NP_002515.1:n.*3366G>T
NM_002524.5:c.*3366G>T MANE Select NP_002515.1:n.*3366G>T
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