Canonical Allele Identifier: CA419887186
Gene: NRAS HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.115256561G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713940G>A , CM000663.2:g.114713940G>A GRCh38
NC_000001.10:g.115256561G>A , CM000663.1:g.115256561G>A GRCh37
NC_000001.9:g.115058084G>A NCBI36
NG_007572.1:g.7955C>T , LRG_92:g.7955C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.150C>T MANE Select ENSP00000358548.4:p.Thr50=
ENST00000369535.4:c.150C>T ENSP00000358548.4:p.Thr50=
NM_002524.4:c.150C>T NP_002515.1:p.Thr50=
NM_002524.5:c.150C>T MANE Select NP_002515.1:p.Thr50=