Canonical Allele Identifier: CA406846042
Gene: RRAS HGNC NCBI

Linked Data

dbSNP Id: rs1238622684
gnomAD v2: 19-50139911-C-T
gnomAD v3: 19-49636654-C-T
gnomAD v4: 19-49636654-C-T
MyVariant Identifiers: chr19:g.50139911C>T (hg19) chr19:g.49636654C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636654C>T , CM000681.2:g.49636654C>T GRCh38
NC_000019.9:g.50139911C>T , CM000681.1:g.50139911C>T GRCh37
NC_000019.8:g.54831723C>T NCBI36
NG_042222.1:g.8490G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.418G>A MANE Select ENSP00000246792.2:p.Val140Ile
ENST00000246792.3:c.418G>A ENSP00000246792.2:p.Val140Ile
ENST00000601532.1:n.558G>A
NM_006270.3:c.418G>A NP_006261.1:p.Val140Ile
NM_006270.4:c.418G>A NP_006261.1:p.Val140Ile
NM_006270.5:c.418G>A MANE Select NP_006261.1:p.Val140Ile
Search 100 bp 5'
Search 100 bp 3'