Canonical Allele Identifier: CA717991894
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs1489784029

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281464C>T , CM000678.2:g.11281464C>T GRCh38
NC_000016.9:g.11375321C>T , CM000678.1:g.11375321C>T GRCh37
NC_000016.8:g.11282822C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+31686C>T
ENST00000572173.1:c.-515-13752C>T ENSP00000461206.1:n.-515-13752C>T
ENST00000573910.1:n.160+31686C>T
XR_933070.1:n.733+31686C>T
XR_933070.3:n.876+31686C>T