Canonical Allele Identifier: CA419886918
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101741757
MyVariant Identifiers: chr1:g.115256432A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713811A>T , CM000663.2:g.114713811A>T GRCh38
NC_000001.10:g.115256432A>T , CM000663.1:g.115256432A>T GRCh37
NC_000001.9:g.115057955A>T NCBI36
NG_007572.1:g.8084T>A , LRG_92:g.8084T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.279T>A MANE Select ENSP00000358548.4:p.Ile93=
ENST00000369535.4:c.279T>A ENSP00000358548.4:p.Ile93=
NM_002524.4:c.279T>A NP_002515.1:p.Ile93=
NM_002524.5:c.279T>A MANE Select NP_002515.1:p.Ile93=