Canonical Allele Identifier: CA885826111
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1312853973
MyVariant Identifiers: chr1:g.115247919T>G (hg19) chr1:g.114705298T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705298T>G , CM000663.2:g.114705298T>G GRCh38
NC_000001.10:g.115247919T>G , CM000663.1:g.115247919T>G GRCh37
NC_000001.9:g.115049442T>G NCBI36
NG_007572.1:g.16597A>C , LRG_92:g.16597A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2796A>C MANE Select ENSP00000358548.4:n.*2796A>C
ENST00000369535.4:c.*2796A>C ENSP00000358548.4:n.*2796A>C
NM_002524.4:c.*2796A>C NP_002515.1:n.*2796A>C
NM_002524.5:c.*2796A>C MANE Select NP_002515.1:n.*2796A>C
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