Canonical Allele Identifier: CA2207547664
Gene: RMI2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11309913T= , CM000678.2:g.11309913T= GRCh38
NC_000016.9:g.11403770T= , CM000678.1:g.11403770T= GRCh37
NC_000016.8:g.11311271T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+60135T=
ENST00000572173.1:c.-436-2916T= ENSP00000461206.1:n.-436-2916T=
ENST00000573910.1:n.161-6539T=
XR_933070.1:n.733+60135T=
XR_933070.3:n.876+60135T=