Canonical Allele Identifier: CA278238581
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs755050081

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11292903del , CM000678.2:g.11292903del GRCh38
NC_000016.9:g.11386760del , CM000678.1:g.11386760del GRCh37
NC_000016.8:g.11294261del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+43125del
ENST00000572173.1:c.-515-2313del ENSP00000461206.1:n.-515-2313del
ENST00000573910.1:n.161-23549del
XR_933070.1:n.733+43125del
XR_933070.3:n.876+43125del