Canonical Allele Identifier: CA419885216
Gene: NRAS HGNC NCBI

Linked Data

gnomAD v4: 1-114709602-A-G
MyVariant Identifiers: chr1:g.115252223A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709602A>G , CM000663.2:g.114709602A>G GRCh38
NC_000001.10:g.115252223A>G , CM000663.1:g.115252223A>G GRCh37
NC_000001.9:g.115053746A>G NCBI36
NG_007572.1:g.12293T>C , LRG_92:g.12293T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.417T>C MANE Select ENSP00000358548.4:p.Ile139=
ENST00000369535.4:c.417T>C ENSP00000358548.4:p.Ile139=
NM_002524.4:c.417T>C NP_002515.1:p.Ile139=
NM_002524.5:c.417T>C MANE Select NP_002515.1:p.Ile139=
Search 100 bp 5'
Search 100 bp 3'