Canonical Allele Identifier: CA633644710

Gene: RRAS

Linked Data

• ClinVar Variation Id: 457989
• ClinVar RCV Id: RCV000547715 ; RCV001755809
• dbSNP Id: rs1490597941
• gnomAD v2: 19-50139118-A-G
• gnomAD v3: 19-49635861-A-G
• gnomAD v4: 19-49635861-A-G
• COSMIC: COSM6292451
• MyVariant Identifiers: chr19:g.50139118A>G (hg19) ; chr19:g.50139118_50139119delinsGG (hg19) ; chr19:g.49635861A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49635861A>G , CM000681.2:g.49635861A>G	GRCh38
NC_000019.9:g.50139118A>G , CM000681.1:g.50139118A>G	GRCh37
NC_000019.8:g.54830930A>G	NCBI36
NG_042222.1:g.9283T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246792.4:c.454-9T>C MANE Select	ENSP00000246792.2:n.454-9T>C
ENST00000246792.3:c.454-9T>C	ENSP00000246792.2:n.454-9T>C
ENST00000601532.1:n.594-9T>C
NM_006270.3:c.454-9T>C	NP_006261.1:n.454-9T>C
NM_006270.4:c.454-9T>C	NP_006261.1:n.454-9T>C
NM_006270.5:c.454-9T>C MANE Select	NP_006261.1:n.454-9T>C