Canonical Allele Identifier: CA752042678

Gene: MIAT

Linked Data

• dbSNP Id: rs1167696139
• gnomAD v3: 22-26662832-A-G
• gnomAD v4: 22-26662832-A-G
• MyVariant Identifiers: chr22:g.27058796A>G (hg19) ; chr22:g.26662832A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.26662832A>G , CM000684.2:g.26662832A>G	GRCh38
NC_000022.10:g.27058796A>G , CM000684.1:g.27058796A>G	GRCh37
NC_000022.9:g.25388796A>G	NCBI36
NG_016621.2:g.10351A>G

Transcript Alleles

HGVS	Amino-acid change
NR_003491.3:n.174-484A>G
NR_033319.2:n.174-484A>G
NR_033320.2:n.174-484A>G
NR_033321.2:n.174-484A>G