Canonical Allele Identifier: CA2207547642
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs2070304603
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11309872C>A , CM000678.2:g.11309872C>A GRCh38
NC_000016.9:g.11403729C>A , CM000678.1:g.11403729C>A GRCh37
NC_000016.8:g.11311230C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+60094C>A
ENST00000572173.1:c.-436-2957C>A ENSP00000461206.1:n.-436-2957C>A
ENST00000573910.1:n.161-6580C>A
XR_933070.1:n.733+60094C>A
XR_933070.3:n.876+60094C>A
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