Canonical Allele Identifier: CA1190291445
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1557982940
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114714305G>A , CM000663.2:g.114714305G>A GRCh38
NC_000001.10:g.115256926G>A , CM000663.1:g.115256926G>A GRCh37
NC_000001.9:g.115058449G>A NCBI36
NG_007572.1:g.7590C>T , LRG_92:g.7590C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-327C>T MANE Select ENSP00000358548.4:n.112-327C>T
ENST00000369535.4:c.112-327C>T ENSP00000358548.4:n.112-327C>T
NM_002524.4:c.112-327C>T NP_002515.1:n.112-327C>T
NM_002524.5:c.112-327C>T MANE Select NP_002515.1:n.112-327C>T
Search 100 bp 5'
Search 100 bp 3'