Canonical Allele Identifier: CA914068584
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs1567477056

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11309984_11309985del , CM000678.2:g.11309984_11309985del GRCh38
NC_000016.9:g.11403841_11403842del , CM000678.1:g.11403841_11403842del GRCh37
NC_000016.8:g.11311342_11311343del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+60206_152+60207del
ENST00000572173.1:c.-436-2845_-436-2844del ENSP00000461206.1:n.-436-2845_-436-2844del
ENST00000573910.1:n.161-6468_161-6467del
XR_933070.1:n.733+60206_733+60207del
XR_933070.3:n.876+60206_876+60207del