Canonical Allele Identifier: CA718010026

Gene: RMI2

Linked Data

• dbSNP Id: rs1382411563
• MyVariant Identifiers: chr16:g.11403848C>G (hg19) ; chr16:g.11309991C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11309991C>G , CM000678.2:g.11309991C>G	GRCh38
NC_000016.9:g.11403848C>G , CM000678.1:g.11403848C>G	GRCh37
NC_000016.8:g.11311349C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649869.1:n.152+60213C>G
ENST00000572173.1:c.-436-2838C>G	ENSP00000461206.1:n.-436-2838C>G
ENST00000573910.1:n.161-6461C>G
XR_933070.1:n.733+60213C>G
XR_933070.3:n.876+60213C>G