Canonical Allele Identifier: CA10779165
Gene: MOV10 HGNC NCBI
COSMIC:
COSN6503087 (not active)
MyVariant.info:
GRCh38 chr1:g.112673921A>G
GRCh37 chr1:g.113216543A>G
gnomAD v2:
1:113216543 A / G
gnomAD v3:
1:112673921 A / G
gnomAD v4:
chr1-112673921-A-G
Joint Max Group AF 0.85389442 (SAS)
Genomes Max Group AF 0.85389442 (SAS)
dbSNP:
2932538
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.112673921A>G , CM000663.2:g.112673921A>G GRCh38
NC_000001.10:g.113216543A>G , CM000663.1:g.113216543A>G GRCh37
NC_000001.9:g.113018066A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000486416.1:n.311+470A>G
Search 100 bp 5'
Search 100 bp 3'