Canonical Allele Identifier: CA278238585
Gene: RMI2 HGNC NCBI

Linked Data

dbSNP Id: rs889163032
MyVariant Identifiers: chr16:g.11386785C>G (hg19) chr16:g.11292928C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11292928C>G , CM000678.2:g.11292928C>G GRCh38
NC_000016.9:g.11386785C>G , CM000678.1:g.11386785C>G GRCh37
NC_000016.8:g.11294286C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649869.1:n.152+43150C>G
ENST00000572173.1:c.-515-2288C>G ENSP00000461206.1:n.-515-2288C>G
ENST00000573910.1:n.161-23524C>G
XR_933070.1:n.733+43150C>G
XR_933070.3:n.876+43150C>G
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