Canonical Allele Identifier: CA1190289546
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1659000058
gnomAD v4: 1-114709814-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709814G>C , CM000663.2:g.114709814G>C GRCh38
NC_000001.10:g.115252435G>C , CM000663.1:g.115252435G>C GRCh37
NC_000001.9:g.115053958G>C NCBI36
NG_007572.1:g.12081C>G , LRG_92:g.12081C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.291-86C>G MANE Select ENSP00000358548.4:n.291-86C>G
ENST00000369535.4:c.291-86C>G ENSP00000358548.4:n.291-86C>G
NM_002524.4:c.291-86C>G NP_002515.1:n.291-86C>G
NM_002524.5:c.291-86C>G MANE Select NP_002515.1:n.291-86C>G
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