Canonical Allele Identifier: CA278238582
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs189295227
gnomAD v2: 16-11386764-C-T
gnomAD v3: 16-11292907-C-T
gnomAD v4: 16-11292907-C-T
MyVariant Identifiers: chr16:g.11386764C>T (hg19) chr16:g.11292907C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11292907C>T , CM000678.2:g.11292907C>T GRCh38
NC_000016.9:g.11386764C>T , CM000678.1:g.11386764C>T GRCh37
NC_000016.8:g.11294265C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+43129C>T
ENST00000572173.1:c.-515-2309C>T ENSP00000461206.1:n.-515-2309C>T
ENST00000573910.1:n.161-23545C>T
XR_933070.1:n.733+43129C>T
XR_933070.3:n.876+43129C>T
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