Canonical Allele Identifier: CA1005998553
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1659002336
gnomAD v3: 1-114709916-G-A
gnomAD v4: 1-114709916-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709916G>A , CM000663.2:g.114709916G>A GRCh38
NC_000001.10:g.115252537G>A , CM000663.1:g.115252537G>A GRCh37
NC_000001.9:g.115054060G>A NCBI36
NG_007572.1:g.11979C>T , LRG_92:g.11979C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.291-188C>T MANE Select ENSP00000358548.4:n.291-188C>T
ENST00000369535.4:c.291-188C>T ENSP00000358548.4:n.291-188C>T
NM_002524.4:c.291-188C>T NP_002515.1:n.291-188C>T
NM_002524.5:c.291-188C>T MANE Select NP_002515.1:n.291-188C>T
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