Canonical Allele Identifier: CA419887198
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1437377780
MyVariant Identifiers: chr1:g.115256579C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713958C>G , CM000663.2:g.114713958C>G GRCh38
NC_000001.10:g.115256579C>G , CM000663.1:g.115256579C>G GRCh37
NC_000001.9:g.115058102C>G NCBI36
NG_007572.1:g.7937G>C , LRG_92:g.7937G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.132G>C MANE Select ENSP00000358548.4:p.Val44=
ENST00000369535.4:c.132G>C ENSP00000358548.4:p.Val44=
NM_002524.4:c.132G>C NP_002515.1:p.Val44=
NM_002524.5:c.132G>C MANE Select NP_002515.1:p.Val44=
Search 100 bp 5'
Search 100 bp 3'