Canonical Allele Identifier: CA278236838
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs541500805
gnomAD v2: 16-11375447-C-T
gnomAD v3: 16-11281590-C-T
gnomAD v4: 16-11281590-C-T
MyVariant Identifiers: chr16:g.11375447C>T (hg19) chr16:g.11281590C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281590C>T , CM000678.2:g.11281590C>T GRCh38
NC_000016.9:g.11375447C>T , CM000678.1:g.11375447C>T GRCh37
NC_000016.8:g.11282948C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+31812C>T
ENST00000572173.1:c.-515-13626C>T ENSP00000461206.1:n.-515-13626C>T
ENST00000573910.1:n.160+31812C>T
XR_933070.1:n.733+31812C>T
XR_933070.3:n.876+31812C>T
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