Canonical Allele Identifier: CA341739106
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1714146
ClinVar RCV Id: RCV002297129
dbSNP Id: rs2101738654
MyVariant Identifiers: chr1:g.115252210T>C (hg19) chr1:g.114709589T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709589T>C , CM000663.2:g.114709589T>C GRCh38
NC_000001.10:g.115252210T>C , CM000663.1:g.115252210T>C GRCh37
NC_000001.9:g.115053733T>C NCBI36
NG_007572.1:g.12306A>G , LRG_92:g.12306A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.430A>G MANE Select ENSP00000358548.4:p.Thr144Ala
ENST00000369535.4:c.430A>G ENSP00000358548.4:p.Thr144Ala
NM_002524.4:c.430A>G NP_002515.1:p.Thr144Ala
NM_002524.5:c.430A>G MANE Select NP_002515.1:p.Thr144Ala
Search 100 bp 5'
Search 100 bp 3'