Canonical Allele Identifier: CA341741640
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs730880965
COSMIC: COSM5351687
MyVariant Identifiers: chr1:g.115256536C>A (hg19) chr1:g.114713915C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713915C>A , CM000663.2:g.114713915C>A GRCh38
NC_000001.10:g.115256536C>A , CM000663.1:g.115256536C>A GRCh37
NC_000001.9:g.115058059C>A NCBI36
NG_007572.1:g.7980G>T , LRG_92:g.7980G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.175G>T MANE Select ENSP00000358548.4:p.Ala59Ser
ENST00000369535.4:c.175G>T ENSP00000358548.4:p.Ala59Ser
NM_002524.4:c.175G>T NP_002515.1:p.Ala59Ser
NM_002524.5:c.175G>T MANE Select NP_002515.1:p.Ala59Ser
Search 100 bp 5'
Search 100 bp 3'