Canonical Allele Identifier: CA974649442

Gene: RMI2

Linked Data

• dbSNP Id: rs988606032
• gnomAD v3: 16-11309920-C-A
• gnomAD v4: 16-11309920-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11309920C>A , CM000678.2:g.11309920C>A	GRCh38
NC_000016.9:g.11403777C>A , CM000678.1:g.11403777C>A	GRCh37
NC_000016.8:g.11311278C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649869.1:n.152+60142C>A
ENST00000572173.1:c.-436-2909C>A	ENSP00000461206.1:n.-436-2909C>A
ENST00000573910.1:n.161-6532C>A
XR_933070.1:n.733+60142C>A
XR_933070.3:n.876+60142C>A