Canonical Allele Identifier: CA309505358

Gene: RRAS

Linked Data

• dbSNP Id: rs1009277194
• gnomAD v2: 19-50139593-G-A
• gnomAD v3: 19-49636336-G-A
• gnomAD v4: 19-49636336-G-A
• MyVariant Identifiers: chr19:g.50139593G>A (hg19) ; chr19:g.49636336G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49636336G>A , CM000681.2:g.49636336G>A	GRCh38
NC_000019.9:g.50139593G>A , CM000681.1:g.50139593G>A	GRCh37
NC_000019.8:g.54831405G>A	NCBI36
NG_042222.1:g.8808C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246792.4:c.453+283C>T MANE Select	ENSP00000246792.2:n.453+283C>T
ENST00000246792.3:c.453+283C>T	ENSP00000246792.2:n.453+283C>T
ENST00000601532.1:n.593+283C>T
NM_006270.3:c.453+283C>T	NP_006261.1:n.453+283C>T
NM_006270.4:c.453+283C>T	NP_006261.1:n.453+283C>T
NM_006270.5:c.453+283C>T MANE Select	NP_006261.1:n.453+283C>T