Canonical Allele Identifier: CA2207547759
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs533536217

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11310063A>T , CM000678.2:g.11310063A>T GRCh38
NC_000016.9:g.11403920A>T , CM000678.1:g.11403920A>T GRCh37
NC_000016.8:g.11311421A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+60285A>T
ENST00000572173.1:c.-436-2766A>T ENSP00000461206.1:n.-436-2766A>T
ENST00000573910.1:n.161-6389A>T
XR_933070.1:n.733+60285A>T
XR_933070.3:n.876+60285A>T