Canonical Allele Identifier: CA885828583
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1320752804
MyVariant Identifiers: chr1:g.115252625A>G (hg19) chr1:g.114710004A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114710004A>G , CM000663.2:g.114710004A>G GRCh38
NC_000001.10:g.115252625A>G , CM000663.1:g.115252625A>G GRCh37
NC_000001.9:g.115054148A>G NCBI36
NG_007572.1:g.11891T>C , LRG_92:g.11891T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.291-276T>C MANE Select ENSP00000358548.4:n.291-276T>C
ENST00000369535.4:c.291-276T>C ENSP00000358548.4:n.291-276T>C
NM_002524.4:c.291-276T>C NP_002515.1:n.291-276T>C
NM_002524.5:c.291-276T>C MANE Select NP_002515.1:n.291-276T>C
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