Canonical Allele Identifier: CA419885202
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101738627
MyVariant Identifiers: chr1:g.115252202G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709581G>C , CM000663.2:g.114709581G>C GRCh38
NC_000001.10:g.115252202G>C , CM000663.1:g.115252202G>C GRCh37
NC_000001.9:g.115053725G>C NCBI36
NG_007572.1:g.12314C>G , LRG_92:g.12314C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.438C>G MANE Select ENSP00000358548.4:p.Ala146=
ENST00000369535.4:c.438C>G ENSP00000358548.4:p.Ala146=
NM_002524.4:c.438C>G NP_002515.1:p.Ala146=
NM_002524.5:c.438C>G MANE Select NP_002515.1:p.Ala146=
Search 100 bp 5'
Search 100 bp 3'