Canonical Allele Identifier: CA718009958
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs1312494189
gnomAD v3: 16-11309856-G-A
gnomAD v4: 16-11309856-G-A
MyVariant Identifiers: chr16:g.11403713G>A (hg19) chr16:g.11309856G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11309856G>A , CM000678.2:g.11309856G>A GRCh38
NC_000016.9:g.11403713G>A , CM000678.1:g.11403713G>A GRCh37
NC_000016.8:g.11311214G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+60078G>A
ENST00000572173.1:c.-436-2973G>A ENSP00000461206.1:n.-436-2973G>A
ENST00000573910.1:n.161-6596G>A
XR_933070.1:n.733+60078G>A
XR_933070.3:n.876+60078G>A
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