Canonical Allele Identifier: CA2207547758
Gene: RMI2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11310063A= , CM000678.2:g.11310063A= GRCh38
NC_000016.9:g.11403920A= , CM000678.1:g.11403920A= GRCh37
NC_000016.8:g.11311421A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+60285A=
ENST00000572173.1:c.-436-2766A= ENSP00000461206.1:n.-436-2766A=
ENST00000573910.1:n.161-6389A=
XR_933070.1:n.733+60285A=
XR_933070.3:n.876+60285A=