Canonical Allele Identifier: CA341739312
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101738756

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709628G>A , CM000663.2:g.114709628G>A GRCh38
NC_000001.10:g.115252249G>A , CM000663.1:g.115252249G>A GRCh37
NC_000001.9:g.115053772G>A NCBI36
NG_007572.1:g.12267C>T , LRG_92:g.12267C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.391C>T MANE Select ENSP00000358548.4:p.His131Tyr
ENST00000369535.4:c.391C>T ENSP00000358548.4:p.His131Tyr
NM_002524.4:c.391C>T NP_002515.1:p.His131Tyr
NM_002524.5:c.391C>T MANE Select NP_002515.1:p.His131Tyr