Canonical Allele Identifier: CA620824230
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs1426622655
gnomAD v2: 16-11375517-A-G
gnomAD v3: 16-11281660-A-G
gnomAD v4: 16-11281660-A-G
MyVariant Identifiers: chr16:g.11375517A>G (hg19) chr16:g.11281660A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281660A>G , CM000678.2:g.11281660A>G GRCh38
NC_000016.9:g.11375517A>G , CM000678.1:g.11375517A>G GRCh37
NC_000016.8:g.11283018A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+31882A>G
ENST00000572173.1:c.-515-13556A>G ENSP00000461206.1:n.-515-13556A>G
ENST00000573910.1:n.160+31882A>G
XR_933070.1:n.733+31882A>G
XR_933070.3:n.876+31882A>G
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