Canonical Allele Identifier: CA885826826
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1472032463
gnomAD v3: 1-114707081-C-T
gnomAD v4: 1-114707081-C-T
MyVariant Identifiers: chr1:g.115249702C>T (hg19) chr1:g.114707081C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707081C>T , CM000663.2:g.114707081C>T GRCh38
NC_000001.10:g.115249702C>T , CM000663.1:g.115249702C>T GRCh37
NC_000001.9:g.115051225C>T NCBI36
NG_007572.1:g.14814G>A , LRG_92:g.14814G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*1013G>A MANE Select ENSP00000358548.4:n.*1013G>A
ENST00000369535.4:c.*1013G>A ENSP00000358548.4:n.*1013G>A
NM_002524.4:c.*1013G>A NP_002515.1:n.*1013G>A
NM_002524.5:c.*1013G>A MANE Select NP_002515.1:n.*1013G>A
Search 100 bp 5'
Search 100 bp 3'