Canonical Allele Identifier: CA717991935
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs1279177864
gnomAD v3: 16-11281532-G-A
gnomAD v4: 16-11281532-G-A
MyVariant Identifiers: chr16:g.11375389G>A (hg19) chr16:g.11281532G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281532G>A , CM000678.2:g.11281532G>A GRCh38
NC_000016.9:g.11375389G>A , CM000678.1:g.11375389G>A GRCh37
NC_000016.8:g.11282890G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+31754G>A
ENST00000572173.1:c.-515-13684G>A ENSP00000461206.1:n.-515-13684G>A
ENST00000573910.1:n.160+31754G>A
XR_933070.1:n.733+31754G>A
XR_933070.3:n.876+31754G>A
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