Canonical Allele Identifier: CA2696726004
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101741703

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713790C>G , CM000663.2:g.114713790C>G GRCh38
NC_000001.10:g.115256411C>G , CM000663.1:g.115256411C>G GRCh37
NC_000001.9:g.115057934C>G NCBI36
NG_007572.1:g.8105G>C , LRG_92:g.8105G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.290+10G>C MANE Select ENSP00000358548.4:n.290+10G>C
ENST00000369535.4:c.290+10G>C ENSP00000358548.4:n.290+10G>C
NM_002524.4:c.290+10G>C NP_002515.1:n.290+10G>C
NM_002524.5:c.290+10G>C MANE Select NP_002515.1:n.290+10G>C