Canonical Allele Identifier: CA996721584

Gene: RRAS

Linked Data

• dbSNP Id: rs2080997078
• gnomAD v3: 19-49636587-A-G
• gnomAD v4: 19-49636587-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49636587A>G , CM000681.2:g.49636587A>G	GRCh38
NC_000019.9:g.50139844A>G , CM000681.1:g.50139844A>G	GRCh37
NC_000019.8:g.54831656A>G	NCBI36
NG_042222.1:g.8557T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246792.4:c.453+32T>C MANE Select	ENSP00000246792.2:n.453+32T>C
ENST00000246792.3:c.453+32T>C	ENSP00000246792.2:n.453+32T>C
ENST00000601532.1:n.593+32T>C
NM_006270.3:c.453+32T>C	NP_006261.1:n.453+32T>C
NM_006270.4:c.453+32T>C	NP_006261.1:n.453+32T>C
NM_006270.5:c.453+32T>C MANE Select	NP_006261.1:n.453+32T>C