Canonical Allele Identifier: CA341741576
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101741948
MyVariant Identifiers: chr1:g.115256506C>A (hg19) chr1:g.114713885C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713885C>A , CM000663.2:g.114713885C>A GRCh38
NC_000001.10:g.115256506C>A , CM000663.1:g.115256506C>A GRCh37
NC_000001.9:g.115058029C>A NCBI36
NG_007572.1:g.8010G>T , LRG_92:g.8010G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.205G>T MANE Select ENSP00000358548.4:p.Asp69Tyr
ENST00000369535.4:c.205G>T ENSP00000358548.4:p.Asp69Tyr
NM_002524.4:c.205G>T NP_002515.1:p.Asp69Tyr
NM_002524.5:c.205G>T MANE Select NP_002515.1:p.Asp69Tyr
Search 100 bp 5'
Search 100 bp 3'