Canonical Allele Identifier: CA278236799

Gene: RMI2

Linked Data

• dbSNP Id: rs991032050
• MyVariant Identifiers: chr16:g.11375225_11375226insG (hg19) ; chr16:g.11281368_11281369insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11281373dup , CM000678.2:g.11281373dup	GRCh38
NC_000016.9:g.11375230dup , CM000678.1:g.11375230dup	GRCh37
NC_000016.8:g.11282731dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000649869.1:n.152+31595dup
ENST00000572173.1:c.-515-13843dup	ENSP00000461206.1:n.-515-13843dup
ENST00000573910.1:n.160+31595dup
XR_933070.1:n.733+31595dup
XR_933070.3:n.876+31595dup