Canonical Allele Identifier: CA2207531839
Gene: RMI2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281558A= , CM000678.2:g.11281558A= GRCh38
NC_000016.9:g.11375415A= , CM000678.1:g.11375415A= GRCh37
NC_000016.8:g.11282916A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+31780A=
ENST00000572173.1:c.-515-13658A= ENSP00000461206.1:n.-515-13658A=
ENST00000573910.1:n.160+31780A=
XR_933070.1:n.733+31780A=
XR_933070.3:n.876+31780A=