Canonical Allele Identifier: CA278236797

Gene: RMI2

Linked Data

• dbSNP Id: rs532935088
• gnomAD v3: 16-11281363-A-C
• gnomAD v4: 16-11281363-A-C
• MyVariant Identifiers: chr16:g.11375220A>C (hg19) ; chr16:g.11281363A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.11281363A>C , CM000678.2:g.11281363A>C	GRCh38
NC_000016.9:g.11375220A>C , CM000678.1:g.11375220A>C	GRCh37
NC_000016.8:g.11282721A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000649869.1:n.152+31585A>C
ENST00000572173.1:c.-515-13853A>C	ENSP00000461206.1:n.-515-13853A>C
ENST00000573910.1:n.160+31585A>C
XR_933070.1:n.733+31585A>C
XR_933070.3:n.876+31585A>C