Canonical Allele Identifier: CA2207538129
Gene: RMI2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11292957T= , CM000678.2:g.11292957T= GRCh38
NC_000016.9:g.11386814T= , CM000678.1:g.11386814T= GRCh37
NC_000016.8:g.11294315T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+43179T=
ENST00000572173.1:c.-515-2259T= ENSP00000461206.1:n.-515-2259T=
ENST00000573910.1:n.161-23495T=
XR_933070.1:n.733+43179T=
XR_933070.3:n.876+43179T=