Canonical Allele Identifier: CA2207538135
Gene: RMI2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11292964C= , CM000678.2:g.11292964C= GRCh38
NC_000016.9:g.11386821C= , CM000678.1:g.11386821C= GRCh37
NC_000016.8:g.11294322C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+43186C=
ENST00000572173.1:c.-515-2252C= ENSP00000461206.1:n.-515-2252C=
ENST00000573910.1:n.161-23488C=
XR_933070.1:n.733+43186C=
XR_933070.3:n.876+43186C=