Canonical Allele Identifier: CA309505489

Gene: RRAS

Linked Data

• dbSNP Id: rs933787543
• gnomAD v2: 19-50139740-A-G
• gnomAD v3: 19-49636483-A-G
• gnomAD v4: 19-49636483-A-G
• MyVariant Identifiers: chr19:g.50139740A>G (hg19) ; chr19:g.49636483A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49636483A>G , CM000681.2:g.49636483A>G	GRCh38
NC_000019.9:g.50139740A>G , CM000681.1:g.50139740A>G	GRCh37
NC_000019.8:g.54831552A>G	NCBI36
NG_042222.1:g.8661T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246792.4:c.453+136T>C MANE Select	ENSP00000246792.2:n.453+136T>C
ENST00000246792.3:c.453+136T>C	ENSP00000246792.2:n.453+136T>C
ENST00000601532.1:n.593+136T>C
NM_006270.3:c.453+136T>C	NP_006261.1:n.453+136T>C
NM_006270.4:c.453+136T>C	NP_006261.1:n.453+136T>C
NM_006270.5:c.453+136T>C MANE Select	NP_006261.1:n.453+136T>C