Canonical Allele Identifier: CA278238580

Gene: RMI2

Linked Data

• dbSNP Id: rs985623110
• gnomAD v3: 16-11292897-G-A
• gnomAD v4: 16-11292897-G-A
• MyVariant Identifiers: chr16:g.11386754G>A (hg19) ; chr16:g.11292897G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11292897G>A , CM000678.2:g.11292897G>A	GRCh38
NC_000016.9:g.11386754G>A , CM000678.1:g.11386754G>A	GRCh37
NC_000016.8:g.11294255G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649869.1:n.152+43119G>A
ENST00000572173.1:c.-515-2319G>A	ENSP00000461206.1:n.-515-2319G>A
ENST00000573910.1:n.161-23555G>A
XR_933070.1:n.733+43119G>A
XR_933070.3:n.876+43119G>A