Canonical Allele Identifier: CA2818611683
Gene: MIAT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26662725G>T , CM000684.2:g.26662725G>T GRCh38
NC_000022.10:g.27058689G>T , CM000684.1:g.27058689G>T GRCh37
NC_000022.9:g.25388689G>T NCBI36
NG_016621.2:g.10244G>T

Transcript Alleles

HGVS Amino-acid Change
NR_003491.3:n.174-591G>T
NR_033319.2:n.174-591G>T
NR_033320.2:n.174-591G>T
NR_033321.2:n.174-591G>T
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