Canonical Allele Identifier: CA9579175
Gene: RRAS HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.49640056G>A
GRCh37 chr19:g.50143313G>A
Revel Score:
ENST00000246792 (MANE Select) 0.075
gnomAD v2:
19:50143313 G / A
gnomAD v3:
19:49640056 G / A
gnomAD v4:
chr19-49640056-G-A
Joint Max Group AF 0.00001681 (SAS)
Exomes Max Group AF 0.00001073 (SAS)
ClinVar RCV:
RCV002471738
ClinVar Variation:
1805320
dbSNP:
544651800
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49640056G>A , CM000681.2:g.49640056G>A GRCh38
NC_000019.9:g.50143313G>A , CM000681.1:g.50143313G>A GRCh37
NC_000019.8:g.54835125G>A NCBI36
NG_042222.1:g.5088C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.43C>T MANE Select ENSP00000246792.2:p.Arg15Trp
ENST00000246792.3:c.43C>T ENSP00000246792.2:p.Arg15Trp
ENST00000601532.1:n.67C>T
NM_006270.3:c.43C>T NP_006261.1:p.Arg15Trp
NM_006270.4:c.43C>T NP_006261.1:p.Arg15Trp
NM_006270.5:c.43C>T MANE Select NP_006261.1:p.Arg15Trp
Search 100 bp 5'
Search 100 bp 3'