Canonical Allele Identifier: CA620826247
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs1339594232

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11310049_11310050del , CM000678.2:g.11310049_11310050del GRCh38
NC_000016.9:g.11403906_11403907del , CM000678.1:g.11403906_11403907del GRCh37
NC_000016.8:g.11311407_11311408del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+60271_152+60272del
ENST00000572173.1:c.-436-2780_-436-2779del ENSP00000461206.1:n.-436-2780_-436-2779de...
ENST00000573910.1:n.161-6403_161-6402del
XR_933070.1:n.733+60271_733+60272del
XR_933070.3:n.876+60271_876+60272del