Canonical Allele Identifier: CA9579029

Gene: RRAS

Linked Data

• ClinVar Variation Id: 457988
• ClinVar RCV Id: RCV000588533 ; RCV001084941 ; RCV002323928
• dbSNP Id: rs114187560
• ExAC: 19:50139921 G / A
• gnomAD v2: 19-50139921-G-A
• gnomAD v3: 19-49636664-G-A
• gnomAD v4: 19-49636664-G-A
• MyVariant Identifiers: chr19:g.50139921G>A (hg19) ; chr19:g.49636664G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49636664G>A , CM000681.2:g.49636664G>A	GRCh38
NC_000019.9:g.50139921G>A , CM000681.1:g.50139921G>A	GRCh37
NC_000019.8:g.54831733G>A	NCBI36
NG_042222.1:g.8480C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000246792.4:c.408C>T MANE Select	ENSP00000246792.2:p.Pro136=
ENST00000246792.3:c.408C>T	ENSP00000246792.2:p.Pro136=
ENST00000601532.1:n.548C>T
NM_006270.3:c.408C>T	NP_006261.1:p.Pro136=
NM_006270.4:c.408C>T	NP_006261.1:p.Pro136=
NM_006270.5:c.408C>T MANE Select	NP_006261.1:p.Pro136=