Canonical Allele Identifier: CA718009992

Gene: RMI2

Linked Data

• dbSNP Id: rs1042930636
• MyVariant Identifiers: chr16:g.11403815C>T (hg19) ; chr16:g.11309958C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11309958C>T , CM000678.2:g.11309958C>T	GRCh38
NC_000016.9:g.11403815C>T , CM000678.1:g.11403815C>T	GRCh37
NC_000016.8:g.11311316C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000649869.1:n.152+60180C>T
ENST00000572173.1:c.-436-2871C>T	ENSP00000461206.1:n.-436-2871C>T
ENST00000573910.1:n.161-6494C>T
XR_933070.1:n.733+60180C>T
XR_933070.3:n.876+60180C>T