Canonical Allele Identifier: CA2207538227
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs2070091203

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11293134dup , CM000678.2:g.11293134dup GRCh38
NC_000016.9:g.11386991dup , CM000678.1:g.11386991dup GRCh37
NC_000016.8:g.11294492dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+43356dup
ENST00000572173.1:c.-515-2082dup ENSP00000461206.1:n.-515-2082dup
ENST00000573910.1:n.161-23318dup
XR_933070.1:n.733+43356dup
XR_933070.3:n.876+43356dup