Canonical Allele Identifier: CA2340507922
Gene: RRAS HGNC NCBI

Linked Data

dbSNP Id: rs1599813574

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636515T>G , CM000681.2:g.49636515T>G GRCh38
NC_000019.9:g.50139772T>G , CM000681.1:g.50139772T>G GRCh37
NC_000019.8:g.54831584T>G NCBI36
NG_042222.1:g.8629A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.453+104A>C MANE Select ENSP00000246792.2:n.453+104A>C
ENST00000246792.3:c.453+104A>C ENSP00000246792.2:n.453+104A>C
ENST00000601532.1:n.593+104A>C
NM_006270.3:c.453+104A>C NP_006261.1:n.453+104A>C
NM_006270.4:c.453+104A>C NP_006261.1:n.453+104A>C
NM_006270.5:c.453+104A>C MANE Select NP_006261.1:n.453+104A>C