Canonical Allele Identifier: CA2207547652
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs2070304873

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11309894A>G , CM000678.2:g.11309894A>G GRCh38
NC_000016.9:g.11403751A>G , CM000678.1:g.11403751A>G GRCh37
NC_000016.8:g.11311252A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+60116A>G
ENST00000572173.1:c.-436-2935A>G ENSP00000461206.1:n.-436-2935A>G
ENST00000573910.1:n.161-6558A>G
XR_933070.1:n.733+60116A>G
XR_933070.3:n.876+60116A>G