Canonical Allele Identifier: CA2207538103
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs2070088928
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11292914T>A , CM000678.2:g.11292914T>A GRCh38
NC_000016.9:g.11386771T>A , CM000678.1:g.11386771T>A GRCh37
NC_000016.8:g.11294272T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+43136T>A
ENST00000572173.1:c.-515-2302T>A ENSP00000461206.1:n.-515-2302T>A
ENST00000573910.1:n.161-23538T>A
XR_933070.1:n.733+43136T>A
XR_933070.3:n.876+43136T>A
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