Canonical Allele Identifier: CA2696725191

Gene: NRAS

Linked Data

• dbSNP Id: rs2101738400

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709480C>G , CM000663.2:g.114709480C>G	GRCh38
NC_000001.10:g.115252101C>G , CM000663.1:g.115252101C>G	GRCh37
NC_000001.9:g.115053624C>G	NCBI36
NG_007572.1:g.12415G>C , LRG_92:g.12415G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.450+89G>C MANE Select	ENSP00000358548.4:n.450+89G>C
ENST00000369535.4:c.450+89G>C	ENSP00000358548.4:n.450+89G>C
NM_002524.4:c.450+89G>C	NP_002515.1:n.450+89G>C
NM_002524.5:c.450+89G>C MANE Select	NP_002515.1:n.450+89G>C