Canonical Allele Identifier: CA620824219
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs1406858152
gnomAD v2: 16-11375365-G-GTGA
MyVariant Identifiers: chr16:g.11375365_11375366insTGA (hg19) chr16:g.11281508_11281509insTGA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281508_11281509insTGA , CM000678.2:g.11281508_11281509insTGA GRCh38
NC_000016.9:g.11375365_11375366insTGA , CM000678.1:g.11375365_11375366insTGA GRCh37
NC_000016.8:g.11282866_11282867insTGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+31730_152+31731insTGA
ENST00000572173.1:c.-515-13708_-515-13707insTGA ENSP00000461206.1:n.-515-13708_-515-13707insTGA
ENST00000573910.1:n.160+31730_160+31731insTGA
XR_933070.1:n.733+31730_733+31731insTGA
XR_933070.3:n.876+31730_876+31731insTGA
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