Canonical Allele Identifier: CA419886903
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101741752
MyVariant Identifiers: chr1:g.115256429G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713808G>A , CM000663.2:g.114713808G>A GRCh38
NC_000001.10:g.115256429G>A , CM000663.1:g.115256429G>A GRCh37
NC_000001.9:g.115057952G>A NCBI36
NG_007572.1:g.8087C>T , LRG_92:g.8087C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.282C>T MANE Select ENSP00000358548.4:p.Asn94=
ENST00000369535.4:c.282C>T ENSP00000358548.4:p.Asn94=
NM_002524.4:c.282C>T NP_002515.1:p.Asn94=
NM_002524.5:c.282C>T MANE Select NP_002515.1:p.Asn94=