Canonical Allele Identifier: CA278243178
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs183839138

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11310077C>T , CM000678.2:g.11310077C>T GRCh38
NC_000016.9:g.11403934C>T , CM000678.1:g.11403934C>T GRCh37
NC_000016.8:g.11311435C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+60299C>T
ENST00000572173.1:c.-436-2752C>T ENSP00000461206.1:n.-436-2752C>T
ENST00000573910.1:n.161-6375C>T
XR_933070.1:n.733+60299C>T
XR_933070.3:n.876+60299C>T