Canonical Allele Identifier: CA2631746389

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281347C>G , CM000678.2:g.11281347C>G GRCh38
NC_000016.9:g.11375204C>G , CM000678.1:g.11375204C>G GRCh37
NC_000016.8:g.11282705C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+31569C>G (RMI2)
ENST00000312511.3:c.-109G>C (PRM1) ENSP00000310515.3:n.-109G>C
ENST00000572173.1:c.-515-13869C>G (RMI2) ENSP00000461206.1:n.-515-13869C>G
ENST00000573910.1:n.160+31569C>G (RMI2)
XR_933070.1:n.733+31569C>G
XR_933070.3:n.876+31569C>G