Canonical Allele Identifier: CA1190284331
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1658884506
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705307G>C , CM000663.2:g.114705307G>C GRCh38
NC_000001.10:g.115247928G>C , CM000663.1:g.115247928G>C GRCh37
NC_000001.9:g.115049451G>C NCBI36
NG_007572.1:g.16588C>G , LRG_92:g.16588C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2787C>G MANE Select ENSP00000358548.4:n.*2787C>G
ENST00000369535.4:c.*2787C>G ENSP00000358548.4:n.*2787C>G
NM_002524.4:c.*2787C>G NP_002515.1:n.*2787C>G
NM_002524.5:c.*2787C>G MANE Select NP_002515.1:n.*2787C>G
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