Canonical Allele Identifier: CA638869682

Gene: MIAT

Linked Data

• gnomAD v2: 22-27058841-T-C
• MyVariant Identifiers: chr22:g.27058841T>C (hg19) ; chr22:g.26662877T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.26662877T>C , CM000684.2:g.26662877T>C	GRCh38
NC_000022.10:g.27058841T>C , CM000684.1:g.27058841T>C	GRCh37
NC_000022.9:g.25388841T>C	NCBI36
NG_016621.2:g.10396T>C

Transcript Alleles

HGVS	Amino-acid change
NR_003491.3:n.174-439T>C
NR_033319.2:n.174-439T>C
NR_033320.2:n.174-439T>C
NR_033321.2:n.174-439T>C