Canonical Allele Identifier: CA2207531794
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs2069952289
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281488C>T , CM000678.2:g.11281488C>T GRCh38
NC_000016.9:g.11375345C>T , CM000678.1:g.11375345C>T GRCh37
NC_000016.8:g.11282846C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+31710C>T
ENST00000572173.1:c.-515-13728C>T ENSP00000461206.1:n.-515-13728C>T
ENST00000573910.1:n.160+31710C>T
XR_933070.1:n.733+31710C>T
XR_933070.3:n.876+31710C>T
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