Canonical Allele Identifier: CA419885208
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs753079400
MyVariant Identifiers: chr1:g.115252208G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709587G>T , CM000663.2:g.114709587G>T GRCh38
NC_000001.10:g.115252208G>T , CM000663.1:g.115252208G>T GRCh37
NC_000001.9:g.115053731G>T NCBI36
NG_007572.1:g.12308C>A , LRG_92:g.12308C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.432C>A MANE Select ENSP00000358548.4:p.Thr144=
ENST00000369535.4:c.432C>A ENSP00000358548.4:p.Thr144=
NM_002524.4:c.432C>A NP_002515.1:p.Thr144=
NM_002524.5:c.432C>A MANE Select NP_002515.1:p.Thr144=
Search 100 bp 5'
Search 100 bp 3'