Canonical Allele Identifier: CA278243078
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs570605855
gnomAD v3: 16-11309913-T-C
gnomAD v4: 16-11309913-T-C
MyVariant Identifiers: chr16:g.11403770T>C (hg19) chr16:g.11309913T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11309913T>C , CM000678.2:g.11309913T>C GRCh38
NC_000016.9:g.11403770T>C , CM000678.1:g.11403770T>C GRCh37
NC_000016.8:g.11311271T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+60135T>C
ENST00000572173.1:c.-436-2916T>C ENSP00000461206.1:n.-436-2916T>C
ENST00000573910.1:n.161-6539T>C
XR_933070.1:n.733+60135T>C
XR_933070.3:n.876+60135T>C
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