Canonical Allele Identifier: CA2340507789
Gene: RRAS HGNC NCBI

Linked Data

dbSNP Id: rs941629057
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636232G>T , CM000681.2:g.49636232G>T GRCh38
NC_000019.9:g.50139489G>T , CM000681.1:g.50139489G>T GRCh37
NC_000019.8:g.54831301G>T NCBI36
NG_042222.1:g.8912C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.454-380C>A MANE Select ENSP00000246792.2:n.454-380C>A
ENST00000246792.3:c.454-380C>A ENSP00000246792.2:n.454-380C>A
ENST00000601532.1:n.594-380C>A
NM_006270.3:c.454-380C>A NP_006261.1:n.454-380C>A
NM_006270.4:c.454-380C>A NP_006261.1:n.454-380C>A
NM_006270.5:c.454-380C>A MANE Select NP_006261.1:n.454-380C>A
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