Canonical Allele Identifier: CA752042622

Gene: MIAT

Linked Data

• dbSNP Id: rs1187564177
• MyVariant Identifiers: chr22:g.27058682C>T (hg19) ; chr22:g.26662718C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.26662718C>T , CM000684.2:g.26662718C>T	GRCh38
NC_000022.10:g.27058682C>T , CM000684.1:g.27058682C>T	GRCh37
NC_000022.9:g.25388682C>T	NCBI36
NG_016621.2:g.10237C>T

Transcript Alleles

HGVS	Amino-acid Change
NR_003491.3:n.174-598C>T
NR_033319.2:n.174-598C>T
NR_033320.2:n.174-598C>T
NR_033321.2:n.174-598C>T