Canonical Allele Identifier: CA2340507804
Gene: RRAS HGNC NCBI

Linked Data

dbSNP Id: rs1599813451

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636278T>C , CM000681.2:g.49636278T>C GRCh38
NC_000019.9:g.50139535T>C , CM000681.1:g.50139535T>C GRCh37
NC_000019.8:g.54831347T>C NCBI36
NG_042222.1:g.8866A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.453+341A>G MANE Select ENSP00000246792.2:n.453+341A>G
ENST00000246792.3:c.453+341A>G ENSP00000246792.2:n.453+341A>G
ENST00000601532.1:n.593+341A>G
NM_006270.3:c.453+341A>G NP_006261.1:n.453+341A>G
NM_006270.4:c.453+341A>G NP_006261.1:n.453+341A>G
NM_006270.5:c.453+341A>G MANE Select NP_006261.1:n.453+341A>G