Canonical Allele Identifier: CA9579112
Gene: RRAS HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.49637030T>C
GRCh37 chr19:g.50140287T>C
gnomAD v2:
19:50140287 T / C
gnomAD v4:
chr19-49637030-T-C
Joint Max Group AF 0.00000359 (NFE)
Exomes Max Group AF 0.00000381 (NFE)
ClinVar RCV:
RCV002193985
ClinVar Variation:
1665962
dbSNP:
765391621
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49637030T>C , CM000681.2:g.49637030T>C GRCh38
NC_000019.9:g.50140287T>C , CM000681.1:g.50140287T>C GRCh37
NC_000019.8:g.54832099T>C NCBI36
NG_042222.1:g.8114A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.241+13A>G MANE Select ENSP00000246792.2:n.241+13A>G
ENST00000246792.3:c.241+13A>G ENSP00000246792.2:n.241+13A>G
ENST00000601532.1:n.278A>G
NM_006270.3:c.241+13A>G NP_006261.1:n.241+13A>G
NM_006270.4:c.241+13A>G NP_006261.1:n.241+13A>G
NM_006270.5:c.241+13A>G MANE Select NP_006261.1:n.241+13A>G
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Search 100 bp 3'