Canonical Allele Identifier: CA885826118
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1359291659
gnomAD v3: 1-114705337-A-C
gnomAD v4: 1-114705337-A-C
MyVariant Identifiers: chr1:g.115247958A>C (hg19) chr1:g.114705337A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705337A>C , CM000663.2:g.114705337A>C GRCh38
NC_000001.10:g.115247958A>C , CM000663.1:g.115247958A>C GRCh37
NC_000001.9:g.115049481A>C NCBI36
NG_007572.1:g.16558T>G , LRG_92:g.16558T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*2757T>G MANE Select ENSP00000358548.4:n.*2757T>G
ENST00000369535.4:c.*2757T>G ENSP00000358548.4:n.*2757T>G
NM_002524.4:c.*2757T>G NP_002515.1:n.*2757T>G
NM_002524.5:c.*2757T>G MANE Select NP_002515.1:n.*2757T>G
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