Canonical Allele Identifier: CA2735887479
Gene: RRAS HGNC NCBI

Linked Data

dbSNP Id: rs941629057
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Genomic Alleles

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

Transcript Alleles

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