Canonical Allele Identifier: CA2696722527
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101743864

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114716017G>C , CM000663.2:g.114716017G>C GRCh38
NC_000001.10:g.115258638G>C , CM000663.1:g.115258638G>C GRCh37
NC_000001.9:g.115060161G>C NCBI36
NG_007572.1:g.5878C>G , LRG_92:g.5878C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.111+33C>G MANE Select ENSP00000358548.4:n.111+33C>G
ENST00000369535.4:c.111+33C>G ENSP00000358548.4:n.111+33C>G
NM_002524.4:c.111+33C>G NP_002515.1:n.111+33C>G
NM_002524.5:c.111+33C>G MANE Select NP_002515.1:n.111+33C>G