Canonical Allele Identifier: CA10779165
Gene: MOV10 HGNC NCBI

Linked Data

dbSNP Id: rs2932538

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