Canonical Allele Identifier: CA2631746579
Gene: RMI2 HGNC NCBI

Linked Data

gnomAD v4: 16-11281435-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281435A>T , CM000678.2:g.11281435A>T GRCh38
NC_000016.9:g.11375292A>T , CM000678.1:g.11375292A>T GRCh37
NC_000016.8:g.11282793A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+31657A>T
ENST00000572173.1:c.-515-13781A>T ENSP00000461206.1:n.-515-13781A>T
ENST00000573910.1:n.160+31657A>T
XR_933070.1:n.733+31657A>T
XR_933070.3:n.876+31657A>T
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