Canonical Allele Identifier: CA718010002

Gene: RMI2

Linked Data

• dbSNP Id: rs1310910505
• MyVariant Identifiers: chr16:g.11403817A>G (hg19) ; chr16:g.11309960A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11309960A>G , CM000678.2:g.11309960A>G	GRCh38
NC_000016.9:g.11403817A>G , CM000678.1:g.11403817A>G	GRCh37
NC_000016.8:g.11311318A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000649869.1:n.152+60182A>G
ENST00000572173.1:c.-436-2869A>G	ENSP00000461206.1:n.-436-2869A>G
ENST00000573910.1:n.161-6492A>G
XR_933070.1:n.733+60182A>G
XR_933070.3:n.876+60182A>G