Canonical Allele Identifier: CA1190289373

Gene: NRAS

Linked Data

• dbSNP Id: rs1658989098

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709368G>C , CM000663.2:g.114709368G>C	GRCh38
NC_000001.10:g.115251989G>C , CM000663.1:g.115251989G>C	GRCh37
NC_000001.9:g.115053512G>C	NCBI36
NG_007572.1:g.12527C>G , LRG_92:g.12527C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.450+201C>G MANE Select	ENSP00000358548.4:n.450+201C>G
ENST00000369535.4:c.450+201C>G	ENSP00000358548.4:n.450+201C>G
NM_002524.4:c.450+201C>G	NP_002515.1:n.450+201C>G
NM_002524.5:c.450+201C>G MANE Select	NP_002515.1:n.450+201C>G