Canonical Allele Identifier: CA2696482967

Gene: NRAS

Linked Data

• dbSNP Id: rs1659156930

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114716044C>A , CM000663.2:g.114716044C>A	GRCh38
NC_000001.10:g.115258665C>A , CM000663.1:g.115258665C>A	GRCh37
NC_000001.9:g.115060188C>A	NCBI36
NG_007572.1:g.5851G>T , LRG_92:g.5851G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000369535.5:c.111+6G>T MANE Select	ENSP00000358548.4:n.111+6G>T
ENST00000369535.4:c.111+6G>T	ENSP00000358548.4:n.111+6G>T
NM_002524.4:c.111+6G>T	NP_002515.1:n.111+6G>T
NM_002524.5:c.111+6G>T MANE Select	NP_002515.1:n.111+6G>T