Canonical Allele Identifier: CA419887154
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101741929
MyVariant Identifiers: chr1:g.115256501T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713880T>C , CM000663.2:g.114713880T>C GRCh38
NC_000001.10:g.115256501T>C , CM000663.1:g.115256501T>C GRCh37
NC_000001.9:g.115058024T>C NCBI36
NG_007572.1:g.8015A>G , LRG_92:g.8015A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.210A>G MANE Select ENSP00000358548.4:p.Gln70=
ENST00000369535.4:c.210A>G ENSP00000358548.4:p.Gln70=
NM_002524.4:c.210A>G NP_002515.1:p.Gln70=
NM_002524.5:c.210A>G MANE Select NP_002515.1:p.Gln70=
Search 100 bp 5'
Search 100 bp 3'