Canonical Allele Identifier: CA278236829
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs892698612

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281529G>T , CM000678.2:g.11281529G>T GRCh38
NC_000016.9:g.11375386G>T , CM000678.1:g.11375386G>T GRCh37
NC_000016.8:g.11282887G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+31751G>T
ENST00000572173.1:c.-515-13687G>T ENSP00000461206.1:n.-515-13687G>T
ENST00000573910.1:n.160+31751G>T
XR_933070.1:n.733+31751G>T
XR_933070.3:n.876+31751G>T