Canonical Allele Identifier: CA309505491

Gene: RRAS

Linked Data

• dbSNP Id: rs553603337
• gnomAD v3: 19-49636487-A-T
• gnomAD v4: 19-49636487-A-T
• MyVariant Identifiers: chr19:g.50139744A>T (hg19) ; chr19:g.49636487A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49636487A>T , CM000681.2:g.49636487A>T	GRCh38
NC_000019.9:g.50139744A>T , CM000681.1:g.50139744A>T	GRCh37
NC_000019.8:g.54831556A>T	NCBI36
NG_042222.1:g.8657T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246792.4:c.453+132T>A MANE Select	ENSP00000246792.2:n.453+132T>A
ENST00000246792.3:c.453+132T>A	ENSP00000246792.2:n.453+132T>A
ENST00000601532.1:n.593+132T>A
NM_006270.3:c.453+132T>A	NP_006261.1:n.453+132T>A
NM_006270.4:c.453+132T>A	NP_006261.1:n.453+132T>A
NM_006270.5:c.453+132T>A MANE Select	NP_006261.1:n.453+132T>A