Canonical Allele Identifier: CA1190289474
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2189829
ClinVar RCV Id: RCV002611852
dbSNP Id: rs1658995392
gnomAD v4: 1-114709563-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709563C>A , CM000663.2:g.114709563C>A GRCh38
NC_000001.10:g.115252184C>A , CM000663.1:g.115252184C>A GRCh37
NC_000001.9:g.115053707C>A NCBI36
NG_007572.1:g.12332G>T , LRG_92:g.12332G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.450+6G>T MANE Select ENSP00000358548.4:n.450+6G>T
ENST00000369535.4:c.450+6G>T ENSP00000358548.4:n.450+6G>T
NM_002524.4:c.450+6G>T NP_002515.1:n.450+6G>T
NM_002524.5:c.450+6G>T MANE Select NP_002515.1:n.450+6G>T
Search 100 bp 5'
Search 100 bp 3'