Canonical Allele Identifier: CA10607593
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 291958
ClinVar RCV Id: RCV000316496 RCV003409430
dbSNP Id: rs150969241
gnomAD v2: 1-115248202-A-T
gnomAD v3: 1-114705581-A-T
gnomAD v4: 1-114705581-A-T
MyVariant Identifiers: chr1:g.115248202A>T (hg19) chr1:g.114705581A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705581A>T , CM000663.2:g.114705581A>T GRCh38
NC_000001.10:g.115248202A>T , CM000663.1:g.115248202A>T GRCh37
NC_000001.9:g.115049725A>T NCBI36
NG_007572.1:g.16314T>A , LRG_92:g.16314T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2513T>A MANE Select ENSP00000358548.4:n.*2513T>A
ENST00000369535.4:c.*2513T>A ENSP00000358548.4:n.*2513T>A
NM_002524.4:c.*2513T>A NP_002515.1:n.*2513T>A
NM_002524.5:c.*2513T>A MANE Select NP_002515.1:n.*2513T>A
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