Canonical Allele Identifier: CA974652419

Gene: RMI2 PRM1

Linked Data

• dbSNP Id: rs2069950323
• gnomAD v3: 16-11281332-A-G
• gnomAD v4: 16-11281332-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11281332A>G , CM000678.2:g.11281332A>G	GRCh38
NC_000016.9:g.11375189A>G , CM000678.1:g.11375189A>G	GRCh37
NC_000016.8:g.11282690A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649869.1:n.152+31554A>G (RMI2)
ENST00000312511.3:c.-94T>C (PRM1)	ENSP00000310515.3:n.-94T>C
ENST00000572173.1:c.-515-13884A>G (RMI2)	ENSP00000461206.1:n.-515-13884A>G
ENST00000573910.1:n.160+31554A>G (RMI2)
NM_002761.2:c.-94T>C (PRM1)	NP_002752.1:n.-94T>C
XR_933070.1:n.733+31554A>G
XR_933070.3:n.876+31554A>G