Canonical Allele Identifier: CA29039821
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs955918025
MyVariant Identifiers: chr1:g.115248106G>C (hg19) chr1:g.114705485G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705485G>C , CM000663.2:g.114705485G>C GRCh38
NC_000001.10:g.115248106G>C , CM000663.1:g.115248106G>C GRCh37
NC_000001.9:g.115049629G>C NCBI36
NG_007572.1:g.16410C>G , LRG_92:g.16410C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*2609C>G MANE Select ENSP00000358548.4:n.*2609C>G
ENST00000369535.4:c.*2609C>G ENSP00000358548.4:n.*2609C>G
NM_002524.4:c.*2609C>G NP_002515.1:n.*2609C>G
NM_002524.5:c.*2609C>G MANE Select NP_002515.1:n.*2609C>G
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