Canonical Allele Identifier: CA1005997027
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1570867789
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705689T>C , CM000663.2:g.114705689T>C GRCh38
NC_000001.10:g.115248310T>C , CM000663.1:g.115248310T>C GRCh37
NC_000001.9:g.115049833T>C NCBI36
NG_007572.1:g.16206A>G , LRG_92:g.16206A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2405A>G MANE Select ENSP00000358548.4:n.*2405A>G
ENST00000369535.4:c.*2405A>G ENSP00000358548.4:n.*2405A>G
NM_002524.4:c.*2405A>G NP_002515.1:n.*2405A>G
NM_002524.5:c.*2405A>G MANE Select NP_002515.1:n.*2405A>G
Search 100 bp 5'
Search 100 bp 3'