Canonical Allele Identifier: CA974657956
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs2070089069
gnomAD v3: 16-11292935-T-C
gnomAD v4: 16-11292935-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11292935T>C , CM000678.2:g.11292935T>C GRCh38
NC_000016.9:g.11386792T>C , CM000678.1:g.11386792T>C GRCh37
NC_000016.8:g.11294293T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+43157T>C
ENST00000572173.1:c.-515-2281T>C ENSP00000461206.1:n.-515-2281T>C
ENST00000573910.1:n.161-23517T>C
XR_933070.1:n.733+43157T>C
XR_933070.3:n.876+43157T>C
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