Canonical Allele Identifier: CA419887171
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101742041
MyVariant Identifiers: chr1:g.115256534A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713913A>T , CM000663.2:g.114713913A>T GRCh38
NC_000001.10:g.115256534A>T , CM000663.1:g.115256534A>T GRCh37
NC_000001.9:g.115058057A>T NCBI36
NG_007572.1:g.7982T>A , LRG_92:g.7982T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.177T>A MANE Select ENSP00000358548.4:p.Ala59=
ENST00000369535.4:c.177T>A ENSP00000358548.4:p.Ala59=
NM_002524.4:c.177T>A NP_002515.1:p.Ala59=
NM_002524.5:c.177T>A MANE Select NP_002515.1:p.Ala59=