Canonical Allele Identifier: CA974652457
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs2069951903

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281463G>C , CM000678.2:g.11281463G>C GRCh38
NC_000016.9:g.11375320G>C , CM000678.1:g.11375320G>C GRCh37
NC_000016.8:g.11282821G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+31685G>C
ENST00000572173.1:c.-515-13753G>C ENSP00000461206.1:n.-515-13753G>C
ENST00000573910.1:n.160+31685G>C
XR_933070.1:n.733+31685G>C
XR_933070.3:n.876+31685G>C