Canonical Allele Identifier: CA2207547716
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs2070305939
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11309996G>T , CM000678.2:g.11309996G>T GRCh38
NC_000016.9:g.11403853G>T , CM000678.1:g.11403853G>T GRCh37
NC_000016.8:g.11311354G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+60218G>T
ENST00000572173.1:c.-436-2833G>T ENSP00000461206.1:n.-436-2833G>T
ENST00000573910.1:n.161-6456G>T
XR_933070.1:n.733+60218G>T
XR_933070.3:n.876+60218G>T
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