Canonical Allele Identifier: CA752042633

Gene: MIAT

Linked Data

• dbSNP Id: rs1256066789
• gnomAD v3: 22-26662732-G-A
• gnomAD v4: 22-26662732-G-A
• MyVariant Identifiers: chr22:g.27058696G>A (hg19) ; chr22:g.26662732G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.26662732G>A , CM000684.2:g.26662732G>A	GRCh38
NC_000022.10:g.27058696G>A , CM000684.1:g.27058696G>A	GRCh37
NC_000022.9:g.25388696G>A	NCBI36
NG_016621.2:g.10251G>A

Transcript Alleles

HGVS	Amino-acid Change
NR_003491.3:n.174-584G>A
NR_033319.2:n.174-584G>A
NR_033320.2:n.174-584G>A
NR_033321.2:n.174-584G>A