Canonical Allele Identifier: CA278236823
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs905157953
MyVariant Identifiers: chr16:g.11281502G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281502G>A , CM000678.2:g.11281502G>A GRCh38
NC_000016.9:g.11375359G>A , CM000678.1:g.11375359G>A GRCh37
NC_000016.8:g.11282860G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+31724G>A
ENST00000572173.1:c.-515-13714G>A ENSP00000461206.1:n.-515-13714G>A
ENST00000573910.1:n.160+31724G>A
XR_933070.1:n.733+31724G>A
XR_933070.3:n.876+31724G>A