Canonical Allele Identifier: CA2696482691
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1658992926
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709492T>A , CM000663.2:g.114709492T>A GRCh38
NC_000001.10:g.115252113T>A , CM000663.1:g.115252113T>A GRCh37
NC_000001.9:g.115053636T>A NCBI36
NG_007572.1:g.12403A>T , LRG_92:g.12403A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.450+77A>T MANE Select ENSP00000358548.4:n.450+77A>T
ENST00000369535.4:c.450+77A>T ENSP00000358548.4:n.450+77A>T
NM_002524.4:c.450+77A>T NP_002515.1:n.450+77A>T
NM_002524.5:c.450+77A>T MANE Select NP_002515.1:n.450+77A>T
Search 100 bp 5'
Search 100 bp 3'