Canonical Allele Identifier: CA278243171
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs1019322928

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11310056G>A , CM000678.2:g.11310056G>A GRCh38
NC_000016.9:g.11403913G>A , CM000678.1:g.11403913G>A GRCh37
NC_000016.8:g.11311414G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+60278G>A
ENST00000572173.1:c.-436-2773G>A ENSP00000461206.1:n.-436-2773G>A
ENST00000573910.1:n.161-6396G>A
XR_933070.1:n.733+60278G>A
XR_933070.3:n.876+60278G>A