Canonical Allele Identifier: CA322664902

Gene: MIAT

Linked Data

• dbSNP Id: rs763314902
• gnomAD v2: 22-27058878-A-T
• gnomAD v3: 22-26662914-A-T
• gnomAD v4: 22-26662914-A-T
• MyVariant Identifiers: chr22:g.27058878A>T (hg19) ; chr22:g.26662914A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.26662914A>T , CM000684.2:g.26662914A>T	GRCh38
NC_000022.10:g.27058878A>T , CM000684.1:g.27058878A>T	GRCh37
NC_000022.9:g.25388878A>T	NCBI36
NG_016621.2:g.10433A>T

Transcript Alleles

HGVS	Amino-acid change
NR_003491.3:n.174-402A>T
NR_033319.2:n.174-402A>T
NR_033320.2:n.174-402A>T
NR_033321.2:n.174-402A>T