Canonical Allele Identifier: CA29042606
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs929794651
gnomAD v2: 1-115252704-C-T
gnomAD v3: 1-114710083-C-T
gnomAD v4: 1-114710083-C-T
MyVariant Identifiers: chr1:g.115252704C>T (hg19) chr1:g.114710083C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114710083C>T , CM000663.2:g.114710083C>T GRCh38
NC_000001.10:g.115252704C>T , CM000663.1:g.115252704C>T GRCh37
NC_000001.9:g.115054227C>T NCBI36
NG_007572.1:g.11812G>A , LRG_92:g.11812G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.291-355G>A MANE Select ENSP00000358548.4:n.291-355G>A
ENST00000369535.4:c.291-355G>A ENSP00000358548.4:n.291-355G>A
NM_002524.4:c.291-355G>A NP_002515.1:n.291-355G>A
NM_002524.5:c.291-355G>A MANE Select NP_002515.1:n.291-355G>A
Search 100 bp 5'
Search 100 bp 3'