Canonical Allele Identifier: CA1190285790
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1658939126

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707277C>G , CM000663.2:g.114707277C>G GRCh38
NC_000001.10:g.115249898C>G , CM000663.1:g.115249898C>G GRCh37
NC_000001.9:g.115051421C>G NCBI36
NG_007572.1:g.14618G>C , LRG_92:g.14618G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*817G>C MANE Select ENSP00000358548.4:n.*817G>C
ENST00000369535.4:c.*817G>C ENSP00000358548.4:n.*817G>C
NM_002524.4:c.*817G>C NP_002515.1:n.*817G>C
NM_002524.5:c.*817G>C MANE Select NP_002515.1:n.*817G>C