Canonical Allele Identifier: CA2647249078
Gene: NRAS HGNC NCBI

Linked Data

gnomAD v4: 1-114716040-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114716040T>G , CM000663.2:g.114716040T>G GRCh38
NC_000001.10:g.115258661T>G , CM000663.1:g.115258661T>G GRCh37
NC_000001.9:g.115060184T>G NCBI36
NG_007572.1:g.5855A>C , LRG_92:g.5855A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.111+10A>C MANE Select ENSP00000358548.4:n.111+10A>C
ENST00000369535.4:c.111+10A>C ENSP00000358548.4:n.111+10A>C
NM_002524.4:c.111+10A>C NP_002515.1:n.111+10A>C
NM_002524.5:c.111+10A>C MANE Select NP_002515.1:n.111+10A>C
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