Canonical Allele Identifier: CA2207531751
Gene: RMI2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281417C= , CM000678.2:g.11281417C= GRCh38
NC_000016.9:g.11375274C= , CM000678.1:g.11375274C= GRCh37
NC_000016.8:g.11282775C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+31639C=
ENST00000572173.1:c.-515-13799C= ENSP00000461206.1:n.-515-13799C=
ENST00000573910.1:n.160+31639C=
XR_933070.1:n.733+31639C=
XR_933070.3:n.876+31639C=