Canonical Allele Identifier: CA717999001
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs1403188590

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11292869C>T , CM000678.2:g.11292869C>T GRCh38
NC_000016.9:g.11386726C>T , CM000678.1:g.11386726C>T GRCh37
NC_000016.8:g.11294227C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+43091C>T
ENST00000572173.1:c.-515-2347C>T ENSP00000461206.1:n.-515-2347C>T
ENST00000573910.1:n.161-23583C>T
XR_933070.1:n.733+43091C>T
XR_933070.3:n.876+43091C>T