Canonical Allele Identifier: CA419885197
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 761147
ClinVar RCV Id: RCV000939169
dbSNP Id: rs1570871392
gnomAD v4: 1-114709575-G-A
MyVariant Identifiers: chr1:g.115252196G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709575G>A , CM000663.2:g.114709575G>A GRCh38
NC_000001.10:g.115252196G>A , CM000663.1:g.115252196G>A GRCh37
NC_000001.9:g.115053719G>A NCBI36
NG_007572.1:g.12320C>T , LRG_92:g.12320C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.444C>T MANE Select ENSP00000358548.4:p.Thr148=
ENST00000369535.4:c.444C>T ENSP00000358548.4:p.Thr148=
NM_002524.4:c.444C>T NP_002515.1:p.Thr148=
NM_002524.5:c.444C>T MANE Select NP_002515.1:p.Thr148=
Search 100 bp 5'
Search 100 bp 3'