Canonical Allele Identifier: CA341741459
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101741836

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713842G>C , CM000663.2:g.114713842G>C GRCh38
NC_000001.10:g.115256463G>C , CM000663.1:g.115256463G>C GRCh37
NC_000001.9:g.115057986G>C NCBI36
NG_007572.1:g.8053C>G , LRG_92:g.8053C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.248C>G MANE Select ENSP00000358548.4:p.Ala83Gly
ENST00000369535.4:c.248C>G ENSP00000358548.4:p.Ala83Gly
NM_002524.4:c.248C>G NP_002515.1:p.Ala83Gly
NM_002524.5:c.248C>G MANE Select NP_002515.1:p.Ala83Gly