Canonical Allele Identifier: CA419885212
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101738673
MyVariant Identifiers: chr1:g.115252217G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709596G>A , CM000663.2:g.114709596G>A GRCh38
NC_000001.10:g.115252217G>A , CM000663.1:g.115252217G>A GRCh37
NC_000001.9:g.115053740G>A NCBI36
NG_007572.1:g.12299C>T , LRG_92:g.12299C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.423C>T MANE Select ENSP00000358548.4:p.Phe141=
ENST00000369535.4:c.423C>T ENSP00000358548.4:p.Phe141=
NM_002524.4:c.423C>T NP_002515.1:p.Phe141=
NM_002524.5:c.423C>T MANE Select NP_002515.1:p.Phe141=
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