Canonical Allele Identifier: CA278236808

Gene: RMI2

Linked Data

• dbSNP Id: rs781527683
• gnomAD v3: 16-11281418-ATGGCCAGG-A
• gnomAD v4: 16-11281418-ATGGCCAGG-A
• MyVariant Identifiers: chr16:g.11375276_11375283del (hg19) ; chr16:g.11281419_11281426del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11281424_11281431del , CM000678.2:g.11281424_11281431del	GRCh38
NC_000016.9:g.11375281_11375288del , CM000678.1:g.11375281_11375288del	GRCh37
NC_000016.8:g.11282782_11282789del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000649869.1:n.152+31646_152+31653del
ENST00000572173.1:c.-515-13792_-515-13785del	ENSP00000461206.1:n.-515-13792_-515-13785...
ENST00000573910.1:n.160+31646_160+31653del
XR_933070.1:n.733+31646_733+31653del
XR_933070.3:n.876+31646_876+31653del