Canonical Allele Identifier: CA122602431

Gene: MIR9-2HG

Linked Data

• dbSNP Id: rs552573182
• gnomAD v2: 5-87968853-G-T
• gnomAD v3: 5-88673035-G-T
• gnomAD v4: 5-88673035-G-T
• MyVariant Identifiers: chr5:g.87968853G>T (hg19) ; chr5:g.88673035G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.88673035G>T , CM000667.2:g.88673035G>T	GRCh38
NC_000005.9:g.87968853G>T , CM000667.1:g.87968853G>T	GRCh37
NC_000005.8:g.88004609G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_015436.1:n.147-7C>A
NR_024383.1:n.99-7C>A
NR_024384.1:n.294C>A
NR_015436.2:n.169-7C>A
NR_024383.2:n.102-7C>A
NR_024384.2:n.305C>A
NR_152232.1:n.185C>A
NR_152233.1:n.130-7C>A
NR_152234.1:n.169-7C>A
NR_152235.1:n.169-1950C>A
NR_152236.1:n.224C>A
NR_152237.1:n.169-1950C>A
NR_152238.1:n.102-7C>A
NR_152239.1:n.102-1950C>A
NR_152240.1:n.908C>A
NR_152241.1:n.114C>A
NR_152242.1:n.305C>A