Canonical Allele Identifier: CA974652505
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs2069952662
gnomAD v3: 16-11281520-G-C
gnomAD v4: 16-11281520-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281520G>C , CM000678.2:g.11281520G>C GRCh38
NC_000016.9:g.11375377G>C , CM000678.1:g.11375377G>C GRCh37
NC_000016.8:g.11282878G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+31742G>C
ENST00000572173.1:c.-515-13696G>C ENSP00000461206.1:n.-515-13696G>C
ENST00000573910.1:n.160+31742G>C
XR_933070.1:n.733+31742G>C
XR_933070.3:n.876+31742G>C
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