Canonical Allele Identifier: CA2631746619
Gene: RMI2 HGNC NCBI

Linked Data

gnomAD v4: 16-11281449-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281449T>A , CM000678.2:g.11281449T>A GRCh38
NC_000016.9:g.11375306T>A , CM000678.1:g.11375306T>A GRCh37
NC_000016.8:g.11282807T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+31671T>A
ENST00000572173.1:c.-515-13767T>A ENSP00000461206.1:n.-515-13767T>A
ENST00000573910.1:n.160+31671T>A
XR_933070.1:n.733+31671T>A
XR_933070.3:n.876+31671T>A
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