Canonical Allele Identifier: CA29042049
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs9724635
gnomAD v3: 1-114709393-C-T
gnomAD v4: 1-114709393-C-T
MyVariant Identifiers: chr1:g.115252014C>T (hg19) chr1:g.114709393C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709393C>T , CM000663.2:g.114709393C>T GRCh38
NC_000001.10:g.115252014C>T , CM000663.1:g.115252014C>T GRCh37
NC_000001.9:g.115053537C>T NCBI36
NG_007572.1:g.12502G>A , LRG_92:g.12502G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.450+176G>A MANE Select ENSP00000358548.4:n.450+176G>A
ENST00000369535.4:c.450+176G>A ENSP00000358548.4:n.450+176G>A
NM_002524.4:c.450+176G>A NP_002515.1:n.450+176G>A
NM_002524.5:c.450+176G>A MANE Select NP_002515.1:n.450+176G>A
Search 100 bp 5'
Search 100 bp 3'