Canonical Allele Identifier: CA341741659
Gene: NRAS HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.115256545G>T (hg19) chr1:g.114713924G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713924G>T , CM000663.2:g.114713924G>T GRCh38
NC_000001.10:g.115256545G>T , CM000663.1:g.115256545G>T GRCh37
NC_000001.9:g.115058068G>T NCBI36
NG_007572.1:g.7971C>A , LRG_92:g.7971C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.166C>A MANE Select ENSP00000358548.4:p.Leu56Met
ENST00000369535.4:c.166C>A ENSP00000358548.4:p.Leu56Met
NM_002524.4:c.166C>A NP_002515.1:p.Leu56Met
NM_002524.5:c.166C>A MANE Select NP_002515.1:p.Leu56Met
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