Canonical Allele Identifier: CA29042542
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs940843535
gnomAD v3: 1-114709912-G-C
gnomAD v4: 1-114709912-G-C
MyVariant Identifiers: chr1:g.115252533G>C (hg19) chr1:g.114709912G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709912G>C , CM000663.2:g.114709912G>C GRCh38
NC_000001.10:g.115252533G>C , CM000663.1:g.115252533G>C GRCh37
NC_000001.9:g.115054056G>C NCBI36
NG_007572.1:g.11983C>G , LRG_92:g.11983C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.291-184C>G MANE Select ENSP00000358548.4:n.291-184C>G
ENST00000369535.4:c.291-184C>G ENSP00000358548.4:n.291-184C>G
NM_002524.4:c.291-184C>G NP_002515.1:n.291-184C>G
NM_002524.5:c.291-184C>G MANE Select NP_002515.1:n.291-184C>G
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