Canonical Allele Identifier: CA9578973
Gene: RRAS HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.49635773T>C
GRCh37 chr19:g.50139030T>C
Revel Score:
ENST00000246792 (MANE Select) 0.388
gnomAD v2:
19:50139030 T / C
gnomAD v4:
chr19-49635773-T-C
Joint Max Group AF 0.00000185 (NFE)
Exomes Max Group AF 0.00000196 (NFE)
ClinVar RCV:
RCV001314034
ClinVar Variation:
1015206
dbSNP:
762794552
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49635773T>C , CM000681.2:g.49635773T>C GRCh38
NC_000019.9:g.50139030T>C , CM000681.1:g.50139030T>C GRCh37
NC_000019.8:g.54830842T>C NCBI36
NG_042222.1:g.9371A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.533A>G MANE Select ENSP00000246792.2:p.Asn178Ser
ENST00000246792.3:c.533A>G ENSP00000246792.2:p.Asn178Ser
NM_006270.3:c.533A>G NP_006261.1:p.Asn178Ser
NM_006270.4:c.533A>G NP_006261.1:p.Asn178Ser
NM_006270.5:c.533A>G MANE Select NP_006261.1:p.Asn178Ser
Search 100 bp 5'
Search 100 bp 3'