Canonical Allele Identifier: CA278243066
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs954148351
gnomAD v2: 16-11403742-A-T
gnomAD v3: 16-11309885-A-T
gnomAD v4: 16-11309885-A-T
MyVariant Identifiers: chr16:g.11403742A>T (hg19) chr16:g.11309885A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11309885A>T , CM000678.2:g.11309885A>T GRCh38
NC_000016.9:g.11403742A>T , CM000678.1:g.11403742A>T GRCh37
NC_000016.8:g.11311243A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+60107A>T
ENST00000572173.1:c.-436-2944A>T ENSP00000461206.1:n.-436-2944A>T
ENST00000573910.1:n.161-6567A>T
XR_933070.1:n.733+60107A>T
XR_933070.3:n.876+60107A>T
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