Canonical Allele Identifier: CA2696722828
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101743904
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114716026C>T , CM000663.2:g.114716026C>T GRCh38
NC_000001.10:g.115258647C>T , CM000663.1:g.115258647C>T GRCh37
NC_000001.9:g.115060170C>T NCBI36
NG_007572.1:g.5869G>A , LRG_92:g.5869G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.111+24G>A MANE Select ENSP00000358548.4:n.111+24G>A
ENST00000369535.4:c.111+24G>A ENSP00000358548.4:n.111+24G>A
NM_002524.4:c.111+24G>A NP_002515.1:n.111+24G>A
NM_002524.5:c.111+24G>A MANE Select NP_002515.1:n.111+24G>A
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