Canonical Allele Identifier: CA885826115
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1404486524
gnomAD v3: 1-114705326-C-T
gnomAD v4: 1-114705326-C-T
MyVariant Identifiers: chr1:g.115247947C>T (hg19) chr1:g.114705326C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705326C>T , CM000663.2:g.114705326C>T GRCh38
NC_000001.10:g.115247947C>T , CM000663.1:g.115247947C>T GRCh37
NC_000001.9:g.115049470C>T NCBI36
NG_007572.1:g.16569G>A , LRG_92:g.16569G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*2768G>A MANE Select ENSP00000358548.4:n.*2768G>A
ENST00000369535.4:c.*2768G>A ENSP00000358548.4:n.*2768G>A
NM_002524.4:c.*2768G>A NP_002515.1:n.*2768G>A
NM_002524.5:c.*2768G>A MANE Select NP_002515.1:n.*2768G>A
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