Canonical Allele Identifier: CA278236798
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs1009707609

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281368A>G , CM000678.2:g.11281368A>G GRCh38
NC_000016.9:g.11375225A>G , CM000678.1:g.11375225A>G GRCh37
NC_000016.8:g.11282726A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+31590A>G
ENST00000572173.1:c.-515-13848A>G ENSP00000461206.1:n.-515-13848A>G
ENST00000573910.1:n.160+31590A>G
XR_933070.1:n.733+31590A>G
XR_933070.3:n.876+31590A>G