Canonical Allele Identifier: CA2207547736
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs2070306546

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11310024T>C , CM000678.2:g.11310024T>C GRCh38
NC_000016.9:g.11403881T>C , CM000678.1:g.11403881T>C GRCh37
NC_000016.8:g.11311382T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+60246T>C
ENST00000572173.1:c.-436-2805T>C ENSP00000461206.1:n.-436-2805T>C
ENST00000573910.1:n.161-6428T>C
XR_933070.1:n.733+60246T>C
XR_933070.3:n.876+60246T>C