Canonical Allele Identifier: CA2207531724
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs1597710760

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281361A>G , CM000678.2:g.11281361A>G GRCh38
NC_000016.9:g.11375218A>G , CM000678.1:g.11375218A>G GRCh37
NC_000016.8:g.11282719A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+31583A>G
ENST00000572173.1:c.-515-13855A>G ENSP00000461206.1:n.-515-13855A>G
ENST00000573910.1:n.160+31583A>G
XR_933070.1:n.733+31583A>G
XR_933070.3:n.876+31583A>G