Canonical Allele Identifier: CA16064899
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 561821
ClinVar RCV Id: RCV000681249
dbSNP Id: rs7549358
gnomAD v2: 1-115252609-G-C
gnomAD v3: 1-114709988-G-C
gnomAD v4: 1-114709988-G-C
MyVariant Identifiers: chr1:g.115252609G>C (hg19) chr1:g.114709988G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709988G>C , CM000663.2:g.114709988G>C GRCh38
NC_000001.10:g.115252609G>C , CM000663.1:g.115252609G>C GRCh37
NC_000001.9:g.115054132G>C NCBI36
NG_007572.1:g.11907C>G , LRG_92:g.11907C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.291-260C>G MANE Select ENSP00000358548.4:n.291-260C>G
ENST00000369535.4:c.291-260C>G ENSP00000358548.4:n.291-260C>G
NM_002524.4:c.291-260C>G NP_002515.1:n.291-260C>G
NM_002524.5:c.291-260C>G MANE Select NP_002515.1:n.291-260C>G
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