Canonical Allele Identifier: CA341739039
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 981572
ClinVar RCV Id: RCV001261091
dbSNP Id: rs2101738617
MyVariant Identifiers: chr1:g.115252197G>A (hg19) chr1:g.114709576G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709576G>A , CM000663.2:g.114709576G>A GRCh38
NC_000001.10:g.115252197G>A , CM000663.1:g.115252197G>A GRCh37
NC_000001.9:g.115053720G>A NCBI36
NG_007572.1:g.12319C>T , LRG_92:g.12319C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.443C>T MANE Select ENSP00000358548.4:p.Thr148Ile
ENST00000369535.4:c.443C>T ENSP00000358548.4:p.Thr148Ile
NM_002524.4:c.443C>T NP_002515.1:p.Thr148Ile
NM_002524.5:c.443C>T MANE Select NP_002515.1:p.Thr148Ile
Search 100 bp 5'
Search 100 bp 3'