Canonical Allele Identifier: CA996721446
Gene: RRAS HGNC NCBI

Linked Data

dbSNP Id: rs2080995543
gnomAD v3: 19-49636210-T-G
gnomAD v4: 19-49636210-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636210T>G , CM000681.2:g.49636210T>G GRCh38
NC_000019.9:g.50139467T>G , CM000681.1:g.50139467T>G GRCh37
NC_000019.8:g.54831279T>G NCBI36
NG_042222.1:g.8934A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.454-358A>C MANE Select ENSP00000246792.2:n.454-358A>C
ENST00000246792.3:c.454-358A>C ENSP00000246792.2:n.454-358A>C
ENST00000601532.1:n.594-358A>C
NM_006270.3:c.454-358A>C NP_006261.1:n.454-358A>C
NM_006270.4:c.454-358A>C NP_006261.1:n.454-358A>C
NM_006270.5:c.454-358A>C MANE Select NP_006261.1:n.454-358A>C
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